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. 2,330 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,330 in last 12 months

Showing 3502135040 of 48,376 recalls

Medical DeviceOctober 21, 2015· Civco Medical Instruments Co. Inc.

Recalled Item: CIVCO Biopsy Starter Kit Recalled by Civco Medical Instruments Co. Inc. Due...

The Issue: Sterility of the product cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· Civco Medical Instruments Co. Inc.

Recalled Item: CIVCO Sales Demo Kit. Large Gauge Infiniti Plus Recalled by Civco Medical...

The Issue: Sterility of the product cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· Civco Medical Instruments Co. Inc.

Recalled Item: CIVCO Needle Guide Starter Kit Recalled by Civco Medical Instruments Co....

The Issue: Sterility of the product cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 6F Recalled by LeMaitre...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 3F Recalled by LeMaitre...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre NovaSil Silicone Single Lumen Embolectomy Catheter 6F Recalled by...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Single Lumen Embolectomy Catheter 4F Recalled by LeMaitre Vascular,...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 4F Recalled by LeMaitre...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Single Lumen Embolectomy Catheter 3F Recalled by LeMaitre Vascular,...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre NovaSil Silicone Single Lumen Embolectomy Catheter 2F Recalled by...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 5F Plus Recalled by LeMaitre...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 5F Plus Recalled by LeMaitre...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Single Lumen Embolectomy Catheter 5F Recalled by LeMaitre Vascular,...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 7F Recalled by LeMaitre...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 3F Recalled by LeMaitre...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· Civco Medical Instruments Co. Inc.

Recalled Item: CIVCO Tracking Bracket Starter Kit Recalled by Civco Medical Instruments Co....

The Issue: Sterility of the product cannot be assured.

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

Class II — Potential Health HazardOngoing
DrugOctober 21, 2015· Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

Recalled Item: RANITIDINE SYRUP (RANITIDINE ORAL SOLUTION Recalled by Vintage...

The Issue: Failed Stability Specifications: Out of Specification results obtained for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 21, 2015· Breckenridge Pharmaceutical, Inc

Recalled Item: Duloxetine Delayed-release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: Presence of Foreign Tablets/Capsules: one foreign capsule identified as...

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

Class III — Low RiskOngoing
Refund
DrugOctober 20, 2015· Teva Pharmaceutical Industries

Recalled Item: Irbesartan and Hydrochlorothiazide tablets USP 150 mg/ 12.5 mg Recalled by...

The Issue: Labeling: Incorrect or Missing Lot AND/OR Exp Date.

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

Class III — Low RiskOngoing
Refund
FoodOctober 20, 2015· Eastland Food Corporation

Recalled Item: Maesri Brand Shrimp Powder Recalled by Eastland Food Corporation Due to The...

The Issue: The New York Department of Agriculture and Markets notified Eastland Food...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund