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. 2,318 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,318 in last 12 months

Showing 3648136500 of 48,376 recalls

Medical DeviceJune 3, 2015· Biomet, Inc.

Recalled Item: Oxford Femoral Drill Guide Lateral IM Adapter Product Usage: Drill Recalled...

The Issue: Oxford Femoral Drill Guide Lateral IM Adapter may have an undersized...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Elite Biomedical Solutions LLC

Recalled Item: Alaris Medley LVP Frame Membrane. Intended use to hold platen Recalled by...

The Issue: Administration of inappropriate quantities of fluid can result, with the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2015· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING ACETABULAR CUP W/IMPACTOR...

The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Stryker Endoscopy

Recalled Item: SERFAS 90 degree Energy Probe Recalled by Stryker Endoscopy Due to Stryker...

The Issue: Stryker Endoscopy is recalling all non expired SERFAS 90 degree Energy...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING FEMORAL HEAD Recalled by...

The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Omnilife Science Inc.

Recalled Item: Apex ARC Hip Stem Recalled by Omnilife Science Inc. Due to Product may...

The Issue: Product may breach the inner and outer sterile pouches during shipping or...

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

Class II — Potential Health HazardOngoing
FoodJune 3, 2015· Centro Naturista

Recalled Item: Smart Lipo Dietary Supplement capsules Recalled by Centro Naturista Due to...

The Issue: Multiple dietary supplement regulation violations.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 2, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker SelectCore Variable Throw Biopsy Device Recalled by Stryker...

The Issue: Stryker Instruments is recalling the Stryker SelectCore Variable Throw...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2015· Alcon Research, Ltd.

Recalled Item: Accurus 2500 Standalone Vitreous Probe Recalled by Alcon Research, Ltd. Due...

The Issue: Insufficient seal on the outside packaging, potentially affecting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2015· ArthroCare Corporation

Recalled Item: EVac 70 XTRA with Integrated Cable and PROcise EZ View Recalled by...

The Issue: Wands inspected with the adaptor fixture were released to the field not...

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

Class II — Potential Health HazardOngoing
DrugJune 2, 2015· The Compounding Pharmacy of America

Recalled Item: Fentanyl 950 mcg/ml + Bupivacaine 5 mg/ml Intrathecal Solution Recalled by...

The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2015· The Compounding Pharmacy of America

Recalled Item: 5-Methy Tetrahydrofolate 5 mg/ml Injectable Recalled by The Compounding...

The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2015· The Compounding Pharmacy of America

Recalled Item: HCG 2 Recalled by The Compounding Pharmacy of America Due to Lack of...

The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2015· The Compounding Pharmacy of America

Recalled Item: Neomycin + Polymyxin B+ Bacitracin Ophthalmic Ointment Recalled by The...

The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2015· The Compounding Pharmacy of America

Recalled Item: Methylcobalamin 1 Recalled by The Compounding Pharmacy of America Due to...

The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2015· The Compounding Pharmacy of America

Recalled Item: Hyaluronidase 150 units/ml Injection Recalled by The Compounding Pharmacy of...

The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2015· The Compounding Pharmacy of America

Recalled Item: Zinc 5 mg/ml Injectable Recalled by The Compounding Pharmacy of America Due...

The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2015· The Compounding Pharmacy of America

Recalled Item: HCG 625 IU/ml Injection Recalled by The Compounding Pharmacy of America Due...

The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2015· The Compounding Pharmacy of America

Recalled Item: Cholecalciferol 600 Recalled by The Compounding Pharmacy of America Due to...

The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2015· The Compounding Pharmacy of America

Recalled Item: Tri-Mix (15 mg/0.5 mg/20 mcg) Injectable Recalled by The Compounding...

The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...

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

Class II — Potential Health HazardOngoing
Refund