Product Recalls in Missouri
Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,747 recalls have been distributed to Missouri in the last 12 months.
Showing 49181–49200 of 52,570 recalls
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOCORD BLUE BRAIDED COMPOSITE SUTURE 2 (5 METRIC) Recalled by DePuy...
The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KEYTABS (Without Iron Recalled by Ancient Formulas Inc Due to Product...
The Issue: Product contains higher levels of niacin than claimed on label .
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bulk tablet label: Keytabs W.O. Glandulars (pink) Recalled by Ancient...
The Issue: Product contains higher levels of niacin than claimed on label .
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: During infusions of 2.0 mL/hr the motor assembly may rotate backwards...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 64 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: If the operator selects a patient name from the worklist using the mouse and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: During infusions of 2.0 mL/hr the motor assembly may rotate backwards...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Children's Acetaminophen Oral Suspension Recalled by Precision Dose Inc. Due...
The Issue: Labeling: Not Elsewhere Classified: This unit dose product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxford Uni Knee System Recalled by Biomet U.K., Ltd. Due to Investigation of...
The Issue: Investigation of complaints found excessive use of the instrument could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HORIBA ABX PENTRA 400 I.S.E. Module Recalled by Horiba Instruments, Inc dba...
The Issue: HORIBA Medical is informing all ABX PENTRA 400 Analyzer with I.S.E. Module...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to Some patients are...
The Issue: Some patients are obtaining access to the dosage reset codes required to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accuray CyberKnife System Medical Physicist Recalled by Accuray Incorporated...
The Issue: A defect on the master-side connector block of the pneumatic tool changer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to Some patients are...
The Issue: Some patients are obtaining access to the dosage reset codes required to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disulfiram Tablets USP 250 mg Recalled by Teva Pharmaceuticals USA, Inc. Due...
The Issue: CGMP Deviation; cotton coil is missing in some packaged bottles
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tizanidine Tablets USP Recalled by Dr. Reddy'S Laboratories Due to Labeling...
The Issue: Labeling Illegible: There is a possibility that the bottle labels do not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxcarbazepine Tablets Recalled by Boehringer Ingelheim Roxane Inc Due to...
The Issue: SubPotent Drug: The firm discovered out of specification results for assay...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Piperacillin and Tazobactam for Injection Recalled by Apotex Corp. Due to...
The Issue: Crystallization: Potential to exhibit precipitation/crystallization in IV...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Camila 0.35 mg Tablets Recalled by Physicians Total Care, Inc. Due to Failed...
The Issue: Failed Impurity/Degradation Specification; an impurity identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cherry Cepacol Sore Throat Lozenges Recalled by Reckitt Benckiser Inc Due to...
The Issue: Subpotent Drug: Product did not conform to the 18-month stability test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.