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. 1,804 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
1,804 in last 12 months

Showing 2256122580 of 48,376 recalls

DrugMarch 5, 2019· AVKARE Inc.

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by AVKARE Inc....

The Issue: CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA)...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 5, 2019· Fenwal Inc

Recalled Item: Fresenius Kabi CATSmart device (Continuous autotransfusion System). Labeled...

The Issue: Based on internal investigations, Fresenius Kabi has identified a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugMarch 4, 2019· Petra Hygienic Systems Int Ltd

Recalled Item: ATHLETICARE Anti-Bacterial Hand Soap AC 550 (triclosan) Recalled by Petra...

The Issue: Does Not Meet Monograph: product contains, triclosan, an ingredient that can...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 1, 2019· American Health Packaging

Recalled Item: Aspirin and Extended-release Dipyridamole Capsules Recalled by American...

The Issue: Failed Impurities/Degradation Specifications; out of specification result...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 1, 2019· AVKARE Inc.

Recalled Item: Oxybutynin Chloride Extended-Release Tablets USP 10 mg Recalled by AVKARE...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 1, 2019· Apotex Inc.

Recalled Item: Drospirenone and Ethinyl Estradiol Tablets Recalled by Apotex Inc. Due to...

The Issue: Contraceptive Tablets Out of Sequence: Missing or incorrect tablet placement.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 1, 2019· Thoratec Corp.

Recalled Item: Thoratec HeartMate 3 Coring Tool Recalled by Thoratec Corp. Due to Small...

The Issue: Small black plastic particle was observed in the left ventricle during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2019· Integra Limited

Recalled Item: Integra bioBLOCK Resorbable subtaler Implant Recalled by Integra Limited Due...

The Issue: Temperature indicator may have changed color to dark gray or black prior to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2019· Integra Limited

Recalled Item: Integra bioBLOCK Resorbable subtaler Implant Recalled by Integra Limited Due...

The Issue: Temperature indicator may have changed color to dark gray or black prior to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2019· Integra Limited

Recalled Item: Integra bioBLOCK Resorbable subtaler Implant Recalled by Integra Limited Due...

The Issue: Temperature indicator may have changed color to dark gray or black prior to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2019· Zimmer Biomet, Inc.

Recalled Item: Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx20mm-Low Profile...

The Issue: Two lengths of the 6.5mm RingLoc Hip System Self-Tapping Bone Screw may have...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2019· Zimmer Biomet, Inc.

Recalled Item: Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx30mm-Low Profile...

The Issue: Two lengths of the 6.5mm RingLoc Hip System Self-Tapping Bone Screw may have...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2019· Medical Action Industries Inc

Recalled Item: Laparotomy Sponge with the following product description and model numbers:...

The Issue: Potential lack of sterility assurance

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugFebruary 28, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium / Hydrochlorothiazide Tablets Recalled by Torrent Pharma...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium / Hydrochlorothiazide Tablets Recalled by Torrent Pharma...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Torrent Pharma Inc.

Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Torrent Pharma Inc.

Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Torrent Pharma Inc.

Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium / Hydrochlorothiazide Tablets Recalled by Torrent Pharma...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2019· Camber Pharmaceuticals Inc

Recalled Item: Losartan Potassium Tablets USP Recalled by Camber Pharmaceuticals Inc Due to...

The Issue: CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund