The firm is recalling all lots of sterile products compounded by the pharmacy that are within expiry.
Lack of Assurance of Sterility: The recall is being initiated due to the lack of sterility assurance and concerns associated with the quality control processes identified during an FDA inspection.
Cornea Coat, Hydroxypropylmethylcellulose, 1.5ml Syringe,  Rx Only. Manufactured by: Insight Instruments, Inc., 2580 SE Willoughby  Blvd., Stuart, FL 34994, USA. Tel: 772-219-9393.
Product was distributed to consumers through firm's website in Florida, Hawaii, California, Illinois, New York, Washington, and Pennsylvania.
HEALTH & BEYOND DR. LARRY'S Tranquility DIETARY SUPPLEMENT 30 Capsules Manufactured for: Health & Beyond 7050 W Palmetto Pk Rd Boca Raton, FL 33433.
Marketed Without an Approved NDA/ANDA; product found to contain Doxepin (an antidepressant) and Chlorpromazine (an antipsychotic)
Dicopanol FusePaq Kit for Oral Suspension, 5mg/ML
Microbial Contamination of Non-Sterile Products: Fusion Pharmaceuticals is recalling the Dicopanol FusePaq Kit due to Total Yeasts and Molds Count above USP limits.
CHILDREN'S IBUPROFEN, ORAL SUSPENSION, 200 mg/10mL cup BERRY FLAVOR, ALCOHOL FREE, MFG: ACTAVIS, PGK BY SAFECOR Columbus, OH
CGMP Deviation: Discoloration; Product fails specification for appearance/color.  A complaint was received regarding an abnormal appearance of children's ibuprofen suspension.
Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75mg/0.2mg, Rx only, Manufactured by Watson Laboratories, Inc., Corona, CA 92880, NDC 0591-0398-60 (60 count bottles)
Failed Tablet/Capsule Specifications: Broken tablets
Cefepime for Injection USP and Dextrose Injection USP, in Duplex Drug Delivery System, 1 g in 50 mL duplex container, For IV Use Only, Single Dose, Sterile/Non pyrogenic, Rx Only, B Braun Medical Inc., NDC 0264-3193-11
Presence of Particulate Matter:  The 1g Cefepime for Injection USP and Dextrose Injection USP lot has been found to contain visible organic particulate matter in a reserve sample unit.
Vet clinics and individual pet owners in Michigan
Unexpired sterile compounded human and veterinary products distributed July 1, 2013 to October 19, 2013 are being recalled after particulate matter, later identified as mold, was found floating in a sterile 50% dextrose product. The recalled products were distributed in Michigan.  If  there is microbial contamination in products intended to be sterile, patients are at risk for serious, potentially life-threatening infections.
CYCLOSPORIN* MCT 0.2% OPHTHALMIC CYCLOSPORIN* MCT 1% OPHTHALMIC   CYCLOSPORIN* MCT 2% OPHTHALMIC
DESMOPRESSIN ACETATE* (0.01%) 0.1MG/ML SOLUTION DESMOPRESSIN ACETATE* (0.0125%) 0.125MG/ML DESMOPRESSIN ACETATE* (0.02%) 0.2MG/ML SOLUTION
TACROLIMUS (VET)* 0.03% OPHTH SOL TACROLIMUS* (VET) 0.02% OPHTH SOL
Unexpired sterile compounded human and veterinary products distributed July 1, 2013 to October 19, 2013 are being recalled after particulate matter, later identified as mold, was found floating in sterile 50% dextrose product. The recalled products were distributed in Michigan.  If  there is microbial contamination in products intended to be sterile, patients are at risk for serious, potentially life-threatening infections.
Blood products, with insufficient plasma to support the platelet concentrations, were distributed.
Blood products, labeled leukoreduced without the assurance that they met the criteria for leukoreduced products, were distributed.
Glipizide XL (glipizide) extended release tablets, 5 mg , 500 count bottles, Rx only, Distributed by: Greenstone Ltd., Peapack, NJ ---  NDC 59762-5032-2
Failed Dissolution Specification; the bulk lot yielded an out of specification result at the 8 hr timepoint, 18 month interval
Glucotrol XL (glipizide) extended release tablets, 5 mg, 100 count bottles, Rx only, Distributed by Roerig, Division of Pfizer Inc, NY, NY --- NDC 0049-1550-66
Failed Dissolution Specification; 8 hr stability timepoint
Nationwide Distribution including CA, MO, PA, NJ, NY, OH, VA, TX, NC, DE, KS, TN, LA, IL, MI, SC, WI, and FL.
Medtronic Advanced Energy Aquamantys3 Pump Generator; Product Catalog Number:  10-1357 (Generator assembly), 40-404-1(as shipped, including accessories) The Aquamantys3 System combines radio frequency (RF) energy and saline to reduce blood loss during and after surgical procedures. This patented Transcollation technology has been shown to reduce transfusion rates and may also reduce the need for other blood management procedures.
lowest serial number is GN001141; the highest is GN001704 (non-consecutive)
The internal protection circuitry on the electrosurgical output that prevents a patient from exposure to DC voltage when the device is activated is being compromised during normal use.
Namenda XR (memantine HCl), 7 mg extended release capsules, 30-count bottle, Rx only, Forest Pharmaceuticals Inc., St. Louis, MO 63045, NDC 0456-3407-33
Failed Dissolution Specifications: Three lots of product being recalled having failed stability dissolution testing.
Namenda XR (memantine HCl), titration pack (7 mg, 14 mg, 21 mg and 28 mg) extended release capsules, packaged in 28-capsule, 4 week, titration pack,Rx only,  Forest Pharmaceuticals Inc., St. Louis, MO 63045  NDC 0456-3400-29.
Namenda XR (memantine HCl), sample pack, 28 mg, extended release capsules, packaged in 5-count sample packs, Rx only,  Forest Pharmaceuticals Inc., St. Louis, MO 63045  NDC 0456-3428-05.
Red Blood Cells (Apheresis) Leukocytes Reduced
Blood products,collected from donors who did not meet the re-entry criteria following invalid NAT testing, were distributed.
Stryker Medical Division of Stryker Corporation
The Gaymar Medi-Therm device provides a means of regulating patient temperature by supplying temperature-controlled water through a connector hose to accessory Gaymar Hyper/Hypothermia blanket(s)/body wrap(s). The blanket/body wrap provides an interface for heating or cooling the patient. Accessory YSI 400 series patient probe interfaces between the Medi-Therm and patient to sense patient temperature, which is displayed on the device's control panel. The Medi-Therm device controls output water temperature by mixing hot and cold water using hot and cold solenoid valves under microprocessor control. The device includes a circulating pump, heater and refrigeration system.  The Medi-Therm controller, connector hose, blanket/body wrap and patient probe comprise the Medi-Therm Hyper/Hypothermia System.
Stryker Medical has identified that on some units of the MTA7900,  there is a lack of a water temperature display while the unit is in Auto mode. While in Auto mode, only the patient temperature is displayed along with the set point. The water display will be blank during Auto mode. If the user wants to see the water temperature displayed and switches out of Auto mode to Manual mode, then back to Auto mode, the therapy will be reset, and may potentially cause patients to reach the set point earlier. The rate of controlled rewarming is a set slope controlled by the Medi-therm unit. There is a potential that the patients passive rate of rewarming is greater than the rate-controlled rewarming. If switched out of Auto mode, the patients passive rewarming is no longer controlled by the machine, which allows the patient to rewarm at their passive rate. Once switched back into Auto mode, the machine will use the patients current temperature as the new starting temperature. The Medi-therm unit will take back control of the rate of warming. However, the patients temperature may potentially have been raised to a higher point while outside of Auto mode due to the patients passive rewarming ability. Consequently, this may result in the patient reaching the target temperature earlier than if modes had not been.
Valacyclovir Hydrochloride Tablets, 1 g, 30 count bottle, Rx only manufactured in Israel by Teva Pharmaceuticals Ind., LTD, Jerusalem, Israel, Manufactured for Teva Pharmaceuticals USA, Sellersville, PA.   NDC #0093-7259-56
Presence of Foreign Tablets/Capsules: Potential of Pravastatin tablet fragments in bottles of Valacyclovir 1 gm Tablets.
50 mg Nitroglycerin in 5% Dextrose Injection (200 mcg/mL), 250 mL glass containers, Baxter Healthcare Corp., Deerfield, IL --- NDC 0338-1049-02
Presence of Particulate Matter; particulate matter in one vial identified as silicone rubber and EPDM rubber from the vial stopper.
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product was distributed to commissaries at Fort Bliss (El Paso, TX) and Holloman Air Force Base (Alamogordo, NM).
Marina's German Bakery; Assorted Pastries; 2 pieces, Minimum Wt. 6 oz. 170 g; UPC# 010801003018; 2033 Trawood Dr., El Paso, Texas 79935
All ''Sell By'' dates, prior to 11/23/2013
The assorted pastry  products may contain undeclared hazelnuts, walnuts or almonds. These tree nuts can cause life-threatening, allergic reactions for some individuals.
Horiba Instruments, Inc dba Horiba Medical
Worldwide Distribution - USA (nationwide)
ABX PENTRA N Control, Model No. A11A01653   The ABX PENTRA N Control is for use in quality control by monitoring accuracy and precision for the quantitative methods as specified in the enclosed annex.
Horiba Medical is recalling the ABX PENTRA N Control because it has been updated to include a revised Target Value assignment for Potassium.
Worldwide Distribution - US Nationwide including Puerto Rico and the countries of:  Australia, Austria, Azerbaijan, Bahrain, Belgium, BRAZIL, Canada, CHILE, COSTA RICA, Cyprus, Czech Republic, Denmark, ECUADOR, Egypt, Estonia, Finland, France, Germany, Greece, GUAM, India, INDONESIA, Iraq, Ireland, Israel, Italy, Japan, Kazakhstan, Korea, Republic of, Kuwait, Lithuania, Malaysia, Malta, Mexico, NEPAL, Netherlands, New Zealand, Norway, Pakistan, PANAMA, PARAGUAY, PERU, Poland, Portugal, Qatar, Romania, Russian Federation, Saudi Arabia, Singapore, Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan, Tanzania, United Republic of, Turkey, United Arab Emirates, United Kingdom, URUGUAY.
CARESCAPE Monitor B850, a multi-parameter high acuity patient monitor intended for use in multiple areas within a professional healthcare facility.     Product Usage:  The CARESCAPE Monitor B850 is intended for use on adult, pediatric, and neonatal patients and on one patient at a time. The CARESCAPE Monitor B850 system is indicated for monitoring of Hemodynamic (including ECG, ST Segment, Arrhythmia Detection, ECG Diagnostic Analysis and Measurement, Invasive Pressure, Noninvasive Blood Pressure, Pulse Oximetry, Cardiac Output, Temperature, Impedance Respiration and SvO2 (Mixed Venous Oxygen Saturation)), Airway Gases (Fi/Et C02, 02, N20 and Anesthetic Agent), Spirometry, Gas Exchange (02 Consumption (VO2), C02 production (VCO2), energy expenditure (BE), and respiratory quotient (RQ)) and neurophysiological (including electroencephalography (EEG), Entropy, Bispectral Index (BIS) and Neuromuscular Transmission (NMT) Monitoring) status. The CARESCAPE Monitor B850 provides alarms, trends, snapshots and events, and calculations and can be connected to displays, printers and recording devices. The CARESCAPE Monitor B850 can be a stand-alone monitor or interfaced to other devices. It can also be connected to other monitors for bed to bed viewing and to data management software devices via a network. The CARESCAPE Monitor B850 is intended for use under the direct supervision of a licensed healthcare practitioner, or by personnel trained in proper use of the equipment in a professional healthcare facility. In addition to the healthcare practitioner, the CARESCAPE Monitor B850 is designed to provide configuration and troubleshooting capabilities to qualified service personnel.
There is a potential for communication loss associated with the F5-01 Frame when connected to CARESCAPE Patient Data Module (PDM) in the CARESCAPE Monitor B850.  The PDM patient parameter acquisition module can sometimes spontaneously lose the communication with the host patient monitor when attached to the F5-01 Frame due to an issue with the PDM Ethernet communication hardware.  The communication loss may occur when the PDM is first attached to the host monitor, or it may lose communication spontaneously during use with no user action.
Blood product, collected from a donor whose suitability to donate was not adequately determined, was distributed.
Blood products, collected on an apheresis machine undergoing validation and which did not have the required quality control testing performed, were distributed.
Fresenius Bicarbonate Jug Adapter to the 2008 Series Hemodialysis machine Part Number: 650103.    The adapter is a socket that accepts the 2008 machine spike to draw concentrate from the container.
Bicarbonate Jug Adapter distributed  prior to 510(k) approval
Faria Limited LLC dba Sheffield Pharmaceuticals
Dr. Sheffield Triple Antibiotic Ointment, OTC a) 0.33 oz (9g) (NDC 11527-162-47); b) 1 oz (22g) (NDC 11527-163-55) SHEFFIELD PHARMACEUTICALS, New London, CT 06320
Microbial Contamination of Non-Sterile Products: Elevated counts of gram positive rods were found during environmental testing
FAMILY wellness Triple Antibiotic Ointment. NET WT 1 OZ (28 g), OTC, DISTRIBUTED BY: FAMILY DOLLAR SERVICES, INC., MATTHEWS,NC 28105
Dollar General Triple Antibiotic Ointment;  NET WT 1 OZ (28 g), OTC, DISTRIBUTED BY DOLGENCORP LLC, GOODLETTSVILLE, TN 37072
Blood products, collected from a donor whose suitability to donate was not adequately determined, were distributed.
Platelets Pheresis Leukocytes Reduced Irradiated
Blood product, which did not meet the platelet QC specification for pH, was distributed.
Michigan; Switzerland; Florida; New York
Blood and Blood Products for Reprocessing
Blood products, tested using a pH meter that had not been calibrated, were distributed.
American National Red Cross (The) - North Central Region
Blood products, labeled leukoreduced without the assurance they met the criteria for leukoreduced products, were distributed.
Blood products, labeled with extended expiration dates, were distributed.
Worldwide Distribution - USA (nationwide) and Internationally to Argentina, Australia,Brazil,Canada, Columbia, China, Ecuador, Egypt, India, Japan, Korea, Mexico, Saudi   Arabia,Singapore, Thailand, and Uruguay.
ADVIA Centaur Systems Phenytoin Calibrator N ( PHTN) 2-pack SMN 10311391    For in vitro diagnostic use in the quantitative determination of phenytoin in serum or plasma using the ADVIA Centaur and ADVIA Centaur XP systems
ADVIA Centaur Systems Phenytoin Calibrator N,  lots CN58 and higher, change in recovery observed with the ADVIA Centaur Systems Phenytoin assay compared to recoveries using previous Calibrator N lots.
ADVIA Centaur Systems Phenytoin Calibrator N ( PHTN)  6-pack SMN 10314977    For in vitro diagnostic use in the quantitative determination of phenytoin in serum or plasma using the ADVIA Centaur and ADVIA Centaur XP systems
Worldwide Distribution - USA (nationwide) and Canada.
ABX PENTRA Urine Control L/H.   The ABX PENTRA Urine Control L/H is a two-level (Low and High) quality control  consisting of liquid solutions prepared from human urine with chemical additives and  materials of biological origin added as required to obtain given component levels. The  assigned values of the control components are given in the labeling, ensuring control of  the appropriate HORIBA ABX SAS methods on the ABX PENTRA chemistry analyzers.  Each control level is provided in one vial of 10 ml.    The ABX PENTRA Urine Control L/H is for use in quality control by monitoring accuracy and precision.
HORIBA Medical is informing all ABX PENTRA Urine Control L/H customers running the Creatinine assay on ABX PENTRA Chemistry Analyzers that the Target Range for Creatinine has been updated. The ABX PENTRA Urine Control L/H lot specific annexes have been updated to  include revised acceptable Target Ranges for Creatinine.No other analyte values  are affected.
Siemens SOMATOM Definition, Definition AS, Definition Flash,  and Definition Edge systems.   X-ray tomography, computed, radiology.
During clinical operation, a malfunction may occur causing a system display freeze with SOMATOM Definition, Definition AS, and definition Edge while running software version syngo CT2012 B and syngo CT2013B.
Worldwide Distribution - USA (nationwide, HI and Puerto Rico and Internationally to Canada, European Union, Jamaica, Suriname, Trinidad and Tobago, Kazakhastan, Russian, Turkey, Australia, Bangladesh, Pakistan, Cambodia, Laos, Myanmar, Thailand, Vietnam, and India.
MooreMedical Supporting Health & Care...MooreBrand Blood Glucose Monitor for Self-Testing & Multi-Patient Use TRUEbalance. Manufactured by: NIPRO DIAGNOSTICS, Fort Lauderdale, FL 33309 U.S.A.   Is intended for the quantitative determination of glucose in human whole blood taken from finger or forearm.
Finished Good: KK0468; Lot Numbers: KL01079, KM0337TI, KN1834TI, KN1973TI, KN2074TI, KN 2089TI, KN2090TI, KN2102TI, KP0047TI, KP0076TI, KP0128TI, KP0925TI.
Manufactured with an incorrect factory set unit of measure.
MooreMedical Supporting Health & Care...MooreBrand Blood Glucose Monitor for Self-Testing & Multi-Patient Use TRUEtrack. Manufactured by: NIPRO DIAGNOSTICS, Fort Lauderdale, FL 33309 U.S.A.   Is intended for the quantitative determination of glucose in human whole blood taken from finger or forearm.
Product was shipped to the following states: AL, AR, AZ, CA, CO, DC, FL, GA, HI, IA, IL, IN, KY, LA, MA, MD, MI, MN, MO, MS, NC, ND, NE, NJ, NV, NY, NY , OH, OR, PA, TN, TX, VA, VT, WA & WI.   Product was also shipped to the following countries: Australia, Belgium, Brazil, Bulgaria, Canada, China, Croatia, Cuba, Denmark, Egypt, France, Germany, Hong Kong, Hungary, India, Indonesia, Italy, Japan, Kuwait, Lebanon, Malta, Mexico, Netherlands, Pakistan, Philippines, Poland, Portugal, Republic of Korea, Russia, Russian Federation, Saudi Arabia, Singapore, Slovakia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, Ukraine, Ukraine, United Kingdom, Venezuela & Vietnam.
Diagnostic imaging systems (GEMINI LXL Model #882412, TruFlight Select Model #882438, GEMINI TF PET/CT16 Model #882470, GEMINI TF PET/CT 64 Model #882471, GEMINI TF Ready Model #882473 & GEMINI TF Big Bore Model #882476)
The PET Reconstruction Server (PRS) database may randomly lock up after the low dose CT acquisition is complete and will not allow the PET acquisition to begin, resulting in an unexpected incomplete study.
US Distribution one importer/wholesale distributor in MO.
B. Braun AccuFlo Elastomeric Infusion Pump 200ML/H 100 ML   Generally used for delivery of antibiotic and local anesthesia medications.
Internal testing of two lots of the AccuFlo CT-2000-100 Elastomeric Infusion Pump identified flow rates which are outside the specified infusion time and may result in overly rapid infusion of medications.
Stryker Instruments Div. of Stryker Corporation
Neptune 2 Rover Ultra Waste Management System.
Manufacturer Part Number 0702-001-000 (120V) All serial numbers
The purpose of this correction is to upgrade the Neptune 2 Waste Management Systems in the field to the recently obtained 510(k) clearance specifications.
Neptune 2 Rover Ultra Waste Management System
Manufacturer Part Number 0702-002-000 (230V) All serial numbers
USA Distribution including the states of : FL, VA, NY, OH, ME, TX, CO, and GA.
***REF 186-01-08***InteGrip ACETABULAR AUGMENT***SMALL 8mm. Use with 48/50mm Shell.***EXACTECH, Gainesville, FL 32653-1630.   The Exactech Novation InteGrip Acetabular Augments are indicated for use in skeletally mature individuals undergoing primary or revision surgery for hip replacement and whose orthopedic surgeon desires a prosthetic alternative to structural allograft in cases of segmental acetabular deficiencies.
Exactech is recalling the InteGrip Acetabular Augments due to an out of range condition for an in-vitro biological evaluation standard.
Worldwide Distribution-USA (nationwide) including DC and Puerto Rico and the states of AL, AK, AZ, CA, CO, CT, DE, FL, GA, IL, IN, KS, KY, LA, ME, MD, MI, MN, MS, MO, MT, NE, NV, NJ, NM, NY, NC, ND, OH, OK, OR, PA, RI, SC, SD, TN, TX, QA, WA, WV, WI, and WY, and the countries of Albania, Algeria, Argentina, Austria, Australia, Bosnia, Bulgaria, Belgium, Bahrain, Brazil, Belarus, Botswana, Bangladesh, Canada, China, Columbia, Costa Rica, Croatia, Cuba, Cyprus, Chile, Czech Republic, Ecuador, Egypt, Estonia, France, Finland, Gabon, Germany, Great Britain, Greece, Guatemala, Hungary, India, Indonesia, Italy, Ireland, Israel, Iraq, Jordan, Japan, Kosovo, Kuwait, Lithuania, Libya, Latvia, Morocco, Malaysia, Malta, Mexico, Myanmar, Netherland, New Zealand, Pakistan, Peru, Philippines, Poland, Portugal, Romania, Russia, Saudi Arabia, Serbia, Singapore, Slovenia, Slovakia, South Africa, South Korea, Spain, Sudan, Syria, Taiwan, Thailand, Turkey, Turkmenistan, Ukraine, Venezuela, and Vietnam.
XiO RTP System.   Used to create treatment plans for any cancer patient for whom external beam radiation therapy or brachytherapy has been prescribed.
When bolus is present, the Effective Depth (with bolus) to the weight point returned on the Source Data Report is incorrect.
Worldwide Distribution-USA (nationwide) including Puerto Rico and the countries of Uruguay, Venezuela, Albania, Algeria, Australia, Austria, Bahrain, Belarus, Belgium, Bolivia, Canada, Chile, China, Costa Rica, Cyprus, Czech Republic, Denmark, Egypt, Estonia, Finland, France, Germany, Greece, Guatemala, Honduras, Hong Kong, Hungary, India, Indonesia, Iraq, Ireland, Israel, Italy, Kazakhstan, Korea, Kuwait, Lithuania, Macedonia, Malaysia, Mexico, Morocco, Netherlands, New Zealand, Nigeria, Norway, Peru, Philippines, Poland, Portugal, Romania, Russia, Saudi Arabia, Singapore, Slovakia, South Africa, Spain, Sweden, Switzerland, Thailand, Tunisia, Turkey, United Arab Emirates, and United Kingdom.
Giraffe Infant Warmers, part number M1118179, labeled in part *** GE Healthcare 8880 Gorman Road Laurel, MD 20723***www.gehealthcare.com*   Giraffe Infant Warmers provide infrared heat in a controlled manner to neonates who are unable to thermo-regulate based on their own physiology.
Medical device adjustment knob may be loose and affect the accuracy of blended Air/Oxygen gas mixture to patients.
Panda iRes Infant Warmers, part number M1112198 and Panda Freestanding Warmers, part number 2063568, labeled in part *** GE Healthcare 8880 Gorman Road Laurel, MD 20723***www.gehealthcare.com**   Panda Infant Warmers provide infrared heat in a controlled manner to neonates who are unable to thermo-regulate based on their own physiology.
Stand-Alone Resuscitation Unit, Bag and Mask, part number M1226444, labeled in part ***GE Healthcare 8880 Gorman Road Laurel, MD 20723***www.gehealthcare.com***.   Provides the basic equipment required for pulmonary resuscitation of infants.
Stand-Alone Resuscitation Unit, Bag and Mask, Upgrade Kits, part number M1139612, labeled in part ***GE Healthcare 8880 Gorman Road Laurel, MD 20723***www.gehealthcare.com***   Provides the basic equipment required for pulmonary resuscitation of infant.s
Stand-Alone Resuscitation, T-Piece, part numbers 2063771-001, 2063772-001, 2063773-001, 2063774-001, 2063775-001, M1226442, M1241420, M1241421, M1241424, M1241425, M1241427, M1241430, M1241461, M1241463, M1241464, and M1241589; labeled in part ***GE Healthcare 8880 Gorman Road Laurel, MD 20723 ***www.gehealthcare.com***    Provides the basic equipment required for pulmonary resuscitation of infants.
Upgrade Kit, Resuscitation, T-Piece, part numbers M1139417, M1192226 and M1223628, labeled in part ***GE Healthcare 8880 Gorman Road Laurel, MD 20723 ***www.gehealthcare.com***   Provides the basic equipment required for pulmonary resuscitation of infants.
Triarco Industries, LLC an Innophos company Multicolor Lightening Drink Granulation Notice - For Manufacturing Use Only Not for Resale
Triarco Industries Inc. is recalling product that may have been contaminated with Chloramphenicol.
Triarco Industries, LLC an Innophos company Red Lightening Drink Granulation  Notice- For manufacturing Use Only Not for Resale
Triarco Industries, LLC an Innophos company Green Lightening Drink Granulation  Notice - For Manufacturing Use Only Not for Resale
Triarco Industries, LLC an Innophos company Activessence (R)  Notice- For Manufacturing Use Only Not for Resale
Worldwide Distribution: US (nationwide) and countries of: Austria, Belgium, Canada, Serbia, Germany, Estonia, Italy, Spain and Saudia Arabia.
Hemochron Jr. Citrate APTT Cuvette 510(k) K014008  A unitized microcoagulation test intended to be used in performing a quantitative, one -stage APTT. The citrate APTT test is used for evaluation of low doses of heparin anticoagulant (up to 1.5 units/mL), depending upon individual patient heparin sensitivity.
25,965 curvettes (7,425 cuvettes US; 18,540 cuvettes OUS)
ITC  has determined that some Citrate APTT cuvettes may recover higher than expected results in normal individuals.
Aztec Cheddar Cheese; Packaged in clear plastic in sizes ranging from 1/2 lb to whole wheels (approximately 13 lbs).  Labeled in part: ''367 BISHOP CHAPEL CHURCH RD  SWAINSBORO, GA  30401***FLAT CREEK LODGE   AZTEC CHEDDAR  Raw milk, salt,***130823XCAZ''
Routine testing by the GA Department of Agriculture revealed  that the firm's Heavenly Blue and Aztec Cheddar products were positive for Salmonella.
Heavenly Blue cheese; Packaged in clear plastic in sizes ranging from 1/2 lb to whole wheels (approximately 8 lbs).  Labeled in part: ''367 BISHOP CHAPEL CHURCH RD  SWAINSBORO, GA 30401***FLAT CREEK LODGE  HEAVENLY BLUE  Raw milk, salt,***130916XHB''.
Medtronic Cardiovascular Surgery-the Heart Valve Division
Product Name: Model 7305- Mosaic Aortic Obturator   The Mosaic Aortic Obturators are used with the Mosaic Porcine Aortic Bioprostheses.
Model 7305.   Lot/Serial Numbers:    The catalog numbers for the Obturator/Sizer are 7305C, 7305UX, and 7305OD.    Scope of this notification includes all Mosaic Obturators/Sizers, used with Mosaic Porcine Aortic  Bioprosthesis implants.
Medtronic, Inc. initiated a recall of Medtronic Mosaic Aortic Obturator Model 7305  used with the Mosaic Porcine Aortic Bioprosthesis, Model Number 305,  because of higher-than-expected transvalvular gradients occurring post implant.
The Rotoprone therapy System is an advanced patient care system for the treatment and prevention of pulmonary complications. The Rotoprone Therapy System provides up to 62 degrees in both prone and supine positions as well as Trendelenburg/Reverse Trendelenburg positioning.     Product Usage:  Use of the Rotoprone Therapy System is indicated for patients with severe acute respiratory distress syndrome (ARDS). These are critical patients who are at higher risk of cardiac arrest and mortality. Placing a patient in the prone position may reopen collapsed airways and thus improve pulmonary gas exchange and respiratory mechanics.
The lock pin can become stuck in the ''in'' position during the manual rotation, resulting in the inability to prone a patient
US Distribution including the states of AL, DC, GA, NY, NJ, OK and PA.
The Symbionic Leg is an integrated prosthetic leg for transfemoral and knee disarticulation amputees.    The prosthesis is composed of the RHEO KNEE and the PROPRIO FOOT, both already existing products from ssur. Both are a battery powered micro-processor controlled prosthetic device and are connected through a shared battery. The knee and the foot have different sensor systems that provide real-time information used to control knee joint resistance and the flexion/extension of the ankle during the gait cycle. Default control parameters are provided with the device but can be manually adjusted by a certified prosthetist through software (knee), or by a certified prosthetist or the user through controls on the device itself (foot).          SYMBIONIC LEG is intended for continuous use by amputees of low to moderate impact levels that weigh less than 125 kg for foot categories 25  30 and less than 100kg for foot Categories 22, 23 and 24. The system is not intended for athletic use.
OSSUR initiated this recall of the Symbionic Leg because it may have a possible defect in a small batch of electronics.
CA, FL, GA, ME, OH, OR, SC, SD, TX and Canada
Patient name displayed (printed) on the Patient Report was the  wrong patient name.
19 customers within WY, 1 customer in MT
Cattle Feed- Tailings and Pulp from beet production
bulk product manufactured from 01/04/14  01/11/14
Product was prepared under insanitary conditions.
Worldwide Distribution - USA including OK, KY, FL, LA, OH, CO, MO, MN and Internationally to Ireland, Saudi Arabia, Italy, Turkey, South Africa, and Germany.
3.5mm Locking Cortical Bone Screw, T15 Hexalobe, Self Tapping, 20mm Part No. 00-0903-2620    OrthoPediatrics Pediloc'' Tibia Plates are indicated for fractures, osteotomies, and non-unions of the pediatric and small stature adult tibia. The subject recalled device is a Bone Screw designed for use with this system.
OrthoPediatrics has initiated a Voluntary RECALL of Part # 00-0903-2620, 3.5MM Locking Cortical Screw, Lot # 009SV because the device within the package may be incorrect.  These packages incorrectly contain a 3.5mm Non Locking Cortical Screw # 00-1050-3524.
LOCATOR Implant Attachment System.   The LOCATOR Implant Attachment System is a universal hinge, resilient attachment for endosseous implants. The LOCATOR Implant Attachment System is designed for use with overdentures or partial dentures, retained in whole or in part, by endosseous implants in the mandible or maxilla.    FDA 510(k): K994257, K072878
Zest Anchors, LLC is voluntarily recalling specific lots of LOCATOR Implant Attachment Systems because it is currently provided with a label that indicates that the final torque applied to the abutment should be 30 N-cm. It was recently noted by Zest that in order to provide an optimal performance by  increasing the factor of safety between the failure load of the abutment screw and the recommended torque, the abutment torque value should be 20 N-cm.
Trifurcated Extension Set, model no. ME 1224. Trifurcated Extension Set, model no. MP 9230.
CareFusion is recalling the Trifurcated Extension Set, models ME 1224 and MP 9230, because they may have a defect in the trifurcated component that could result in a component leak.
PROVENGE, which did not meet the release spec for CD54 upregulation, or which had the potential to not meet the potency release specification for CD54 upregulation, was distributed.
Worldwide Distribution: US (nationwide) including Puerto Rico; and internationally to: Australia, Canada and New Zealand.
SmartSite Needleless Connector, Model No. 2000E    The SmartSite Needleless Connectors are sterile, individually packaged connectors. The connectors are used to administer fluid and medications. The needle free connector allows the user to add medication into the primary line without the use of a needle.
CareFusion is recalling the SmartSite Needlefree Connector, model number 2000E, because of connection issues.  The affected SmartSite connector lots may unintentionally disconnect from a female luer, may be difficult to disconnect from a female luer, or may fail to disconnect from a female luer once attached.  Leakage may also be observed if the connector disconnects from the female luer during infusion.
Worldwide distribution: US (nationwide) including Guam and DC but excluding CT, DE, HI and RI; and internationally to: AUSTRALIA, BULGARIA, CANADA, CHILE, DOMINICAN REPUBLIC, GERMANY, HONDURAS, IRELAND, ITALY, KUWAIT, LEBANON, MALTA, NAMIBIA, PORTUGAL, ROMANIA, RUSSIA, SAUDI ARABIA, SLOVAKIA, SPAIN, SWITZERLAND, TAIWAN, TURKEY, UNITED KINGDOM, VENEZUELA, and YEMEN.
GE Healthcare Precision 500D, Precision MPI & Precision RXI X-ray imaging systems.   The Precision 500D R&F X-ray System is intended to be used as a universal diagnostic imaging system for radiographic and fluoroscopic examinations, including general R&F and pediatric examinations. The Precision 500D R&F X-ray Systems are intended for use by a qualified/trained doctor or technician on both adult and pediatric subjects for taking diagnostic radiographic and fluoroscopic exposures of the whole body, skull, spinal column, chest, abdomen, extremities, and other body parts. Applications can be performed with the patient sitting, standing, or lying in the prone or supine position.
GE Healthcare has recently become aware of a potential safety issue involving the Precision 500D, Precision MPI & Precision RXI X-ray imaging systems overhead LCD Video Monitor Suspension (Single monitor & Dual monitor).   There is a potential for the locking nut to loosen out of the LCD Video Monitor Suspension yoke. This will not lead to an immediate fall of the suspended monitor since it will be held in place by the remaining bushing and a screw in the absence of  the locking-nut. To date, no injury has been reported due to this.
Crimper Model 9100CR26   The Crimper is indicated for use in preparing the Edwards SAPIEN Transcatheter Heart Valve for implantation.
Edwards Lifesciences is recalling two lot numbers of the 26mm transcatheter heart valve crimper because they may not open sufficiently when the handle is rotated in the full open position. As a result, user may have difficulty fitting a 26mm Sapien transcatheter heart valve into the crimper orifice when preparing the valve for crimping.
Lenguita Cookies net wt. 6 oz., Distributed by Mama Lycha Foods, Houston TX 77055 toll free (877)MAMALYCHA email contact@mamalycha.com www.mamalycha.com Product of Honduras
Worldwide Distribution - USA including IL, KY, MI, NY, CA, FL, LA and Internationally to Switzerland., Denmark, Greece, Australia, England, and Canada.
SuperElastic Regular force NiTi lower or upper Natural arches. 0.16 size  10 or 100 count packages.  Highland Metals Inc.  San Jose, CA     The devices are intended to provide force to the teeth to effect movement in order to alter their position.
Part Number         Part Description         Lot Number    Label Form    Actual Form 11100161124     SE Niti 016 Nat U 100     41684                 Upper         Lower  11100161125     SE Niti 016 Nat U 10        41684                 Upper        Lower  11100161144     SE Niti 016 Nat L 100      41679                 Lower         Upper
Labeling issue: Product labeled as ''Upper'' may contain ''Lower'' archwires with a red midline mark. Product labeled ad ''Lower'' may contain ''Upper'' archwires with a black midline mark.
SuperElastic Regular force NiTi lower or upper Natural arches. 0.14 size  10 or 100 count packages.  Highland Metals Inc.  San Jose, CA     The devices are intended to provide force to the teeth to effect movement in order to alter their position.
Part Number         Part Description         Lot Number    Label Form    Actual Form 11100141124   SE Niti 014 Nat U 100     41756                Upper         Lower           11100141144   SE Niti 014 Nat L 100      41760                 Lower         Upper  11100141145   SE Niti 014 Nat L 10        41760                 Lower         Upper