Product Recalls in West Virginia
Product recalls affecting West Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to West Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,380 recalls have been distributed to West Virginia in the last 12 months.
Showing 21201–21220 of 48,376 recalls
Recalled Item: Losartan Potassium Tablets 50 mg 1000 Tablets Recalled by Macleods Pharma...
The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by Macleods...
The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets Recalled by Macleods Pharma Usa Inc Due to CGMP...
The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by Macleods...
The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium andHydrochlorothiazide Tablets 100 mg/25 mg 90 tablets...
The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Parent's Choice Advantage Infant Formula Milk-Based Powder with Iron...
The Issue: Product may contain metal fragments.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Norm-O-Temp model 111Z Recalled by Cincinnati Sub-Zero Products LLC, a...
The Issue: The manual does not provide instruction stating that exceeding 40 Celsius...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norm-O-Temp model 111W Recalled by Cincinnati Sub-Zero Products LLC, a...
The Issue: The manual does not provide instruction stating that exceeding 40 Celsius...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TURBO DROPS (PHEN 10% / CYCLO 1%/ TROP 1%/ KETO 0.5%) OPHTH SOLN Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROXOCOBALAMIN 1000 MCG/ML (MDV) Recalled by RXQ Compounding LLC Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KETAMINE 10 MG/ML INJ SOL SYR (C-III) Recalled by RXQ Compounding LLC Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TURBO CAINE 2.5 (PHEN2.5/CYCLO1/ TROP1/TETRA 0.5) Recalled by RXQ...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GLUTATHIONE 200MG/ML (MDV) INJECTION SOLN Recalled by RXQ Compounding LLC...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITAMIN B COMPLEX 100 (MDV) Recalled by RXQ Compounding LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.