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. 2,266 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,266 in last 12 months

Showing 4644146460 of 48,376 recalls

Medical DeviceSeptember 28, 2012· Biomet 3i, LLC

Recalled Item: Product is Full OSSEOTITE Parallel Walled Certain Implant Recalled by Biomet...

The Issue: Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2012· Biomet 3i, LLC

Recalled Item: Product is Full OSSEOTITE 2 Tapered Certain Implant Recalled by Biomet 3i,...

The Issue: Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2012· Synthes USA HQ, Inc.

Recalled Item: Synthes External Fixation System Tube to Tube Clamp Recalled by Synthes USA...

The Issue: The insert provided with the product for the specific lot number indicates...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2012· ICU Medical, Inc.

Recalled Item: 3 PORT "OFF" MANIFOLD w/WASTE BAG Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical, Inc. has identified a potential comingling of components where...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2012· Encore Medical, Lp

Recalled Item: 6.5mm Cancellous Bone Screw Intended to be used for the Recalled by Encore...

The Issue: A product complaint was received where a size 20 screw was labeled as size...

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

Class II — Potential Health HazardOngoing
DrugSeptember 27, 2012· Fresenius Kabi USA, LLC

Recalled Item: CYANOCOBALAMIN INJECTION Recalled by Fresenius Kabi USA, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility: Glass vials may have finish fractures and...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2012· Fresenius Kabi USA, LLC

Recalled Item: MIDAZOLAM HYDROCHLORIDE INJECTION Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Lack of Assurance of Sterility: Glass vials may have finish fractures and...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2012· Fresenius Kabi USA, LLC

Recalled Item: ONDANSETRON INJECTION Recalled by Fresenius Kabi USA, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility: Glass vials may have finish fractures and...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2012· Genentech, Inc.

Recalled Item: CellCept (mycophenolate mofetil) capsules Recalled by Genentech, Inc. Due to...

The Issue: Short Fill: some bottles contained less than 120-count per labeled claim.

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2012· Dr. Reddy's Laboratories, Inc.

Recalled Item: Dr. Reddy's Quetiapine Fumarate Tablets Recalled by Dr. Reddy's...

The Issue: Failed USP Dissolution Test Requirements: During analysis of long term...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 27, 2012· Harry and David Operations, Inc.

Recalled Item: Harry & David Creamy Caramel Peanut Spread Recalled by Harry and David...

The Issue: Product received from supplier is being recalled due to the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 27, 2012· Harry and David Operations, Inc.

Recalled Item: Harry & David Creamy Raspberry Peanut Spread Recalled by Harry and David...

The Issue: Product received from supplier is being recalled due to the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 27, 2012· Harry and David Operations, Inc.

Recalled Item: Harry & David Creamy Banana Peanut Spread Recalled by Harry and David...

The Issue: Product received from supplier is being recalled due to the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 27, 2012· Harry and David Operations, Inc.

Recalled Item: Harry & David Crunchy Almond and Peanut Butter Recalled by Harry and David...

The Issue: Product received from supplier is being recalled due to the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 27, 2012· Newman's Own Organics

Recalled Item: Newman's Own Organics brand Newman-O's Peanut Butter Creme Filled Chocolate...

The Issue: The product was manufactured using peanut butter recalled by Sunland Inc....

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 27, 2012· Cellestis Inc

Recalled Item: Vacuette Cellestis 1 ml QuantiFERON¿ TB ANTIGEN (HA) High Altitude: Shake...

The Issue: Cellestis is recalling QuantiFERON¿¿ - TB Gold TB Blood Collection Tubes and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2012· Cellestis Inc

Recalled Item: VACUETTE Cellestis 1 ml QuantiFERON¿ - TB ANTIGEN Recalled by Cellestis Inc...

The Issue: Cellestis is recalling QuantiFERON¿¿ - TB Gold TB Blood Collection Tubes and...

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

Class II — Potential Health HazardOngoing
DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Methylprednisolone Acetate (PF) 40 mg/ml Injection Recalled by New England...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Glycerin 100% PF Recalled by New England Compounding Center Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Methylprednisolone Acetate 40 mg/mL Injection Recalled by New England...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund