Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,279 recalls have been distributed to Wyoming in the last 12 months.
Showing 45181–45200 of 48,219 recalls
Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by Watson...
The Issue: Failed Tablet/Capsule Specifications: Broken tablets
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended-Release Tablets (XL) 300 mg Recalled by...
The Issue: Failed USP Dissolution Test Requirements: Out-of-specification dissolution...
Recommended Action: Stop taking this medication. Contact your pharmacy or 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: 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: 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: 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: 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: 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.
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: Donnatal Extentabs Recalled by West-ward Pharmaceutical Corp. Due to...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Bottled product is...
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: Ethambutol Hydrochloride Tablets Recalled by West-ward Pharmaceutical Corp....
The Issue: Subpotent Drug: Out Of Specification results for assay at the stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LeMaitre Stent Guide: 1102-00 (100 strips) Recalled by LeMaitre Vascular,...
The Issue: Devices were not sealed correctly during the manufacturing process, and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar Pump - Battery Product Usage: The GemStar Pump is Recalled by...
The Issue: Battery level lower then 2.4 volts results in corrupt history log and loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.