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. 1,658 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
1,658 in last 12 months

Showing 4332143340 of 48,376 recalls

Medical DeviceAugust 30, 2013· Zimmer, Inc.

Recalled Item: NexGen¿ Femoral Component (CR-FLEX GSF PRECOAT SZ C-L Recalled by Zimmer,...

The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT Big Bore Oncology Recalled by Philips Medical Systems...

The Issue: There are artifacts appearing on the Tracker images during...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· Zimmer, Inc.

Recalled Item: Zimmer¿ Unicompartmental Knee Femoral Component. Indicated for patients with...

The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· Zimmer, Inc.

Recalled Item: Gender Solutions" Patello-Femoral Component Recalled by Zimmer, Inc. Due to...

The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· Zimmer, Inc.

Recalled Item: CoCr Head (Not distributed in the United States) Used in Recalled by Zimmer,...

The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· Zimmer, Inc.

Recalled Item: Natural-Knee¿ Flex Femoral Component. Provides increased flexion capability....

The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Emit 2000 Phenobarbital Assay and Syva Emit 2000 Phenobarbital Assay...

The Issue: Imprecision with certain lots

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: Combiset Blood Line with BVM for Hemodialysis use Catalog Number: Recalled...

The Issue: Updated Instructions for Use: Bloodline connections not tightened per...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: Combiset Blood Line Hemodialysis use Catalog Number: 03-2622-3. Intended for...

The Issue: Updated Instructions for Use: Bloodline connections not tightened per...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Vital Diagnostics, Inc.

Recalled Item: Vital Diagnostics Envoy Calcium Reagent For In-Vitro Diagnostic Use. PN...

The Issue: High positive calcium bias on plasma sample versus results on serum

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008K@ Home Blood lines Combiset True Flow Series for Hemodialysis Recalled...

The Issue: Updated Instructions for Use: Bloodline connections not tightened per...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Carestream Health Inc.

Recalled Item: DRX- Revolution Recalled by Carestream Health Inc. Due to Carestream Health...

The Issue: Carestream Health Inc. has conducted a voluntary field action which includes...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek FMS Outflow Tubing with One-Way valve Product Code:284649...

The Issue: Pillow valve included in the FMS Duo outflow tubing set and the FMS Solo...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Carestream Health Inc.

Recalled Item: Carestream DRX-Revolution Mobile X-Ray System -- Made in U.S.A. by Recalled...

The Issue: It was discovered that Carestream received a report from a customer that 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek FMS Intermediary Tubing with One-Way valve Product Code:...

The Issue: Pillow valve included in the FMS Duo outflow tubing set and the FMS Solo...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Carestream Health Inc.

Recalled Item: CARESTREAM DRX -Mobile Retrofit Kit Recalled by Carestream Health Inc. Due...

The Issue: Carestream Health Inc. has conducted a voluntary field action which includes...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Vital Diagnostics, Inc.

Recalled Item: Consult Diagnostics¿ Eon Calcium Reagent For In-Vitro Diagnostic Use PN:...

The Issue: High positive calcium bias on plasma sample versus results on serum

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

Class II — Potential Health HazardOngoing
DrugAugust 29, 2013· Procter & Gamble Co

Recalled Item: Vicks NyQuil Cold and Flu Nighttime Relief Recalled by Procter & Gamble Co...

The Issue: Incorrect/ Undeclared Excipients: NyQuil Liquid Original bottles were...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2013· Hospira Inc.

Recalled Item: 5% Lidocaine HCl and 7.5% Dextrose Injection Recalled by Hospira Inc. Due to...

The Issue: Presence of Particulate Matter; report of visible particulates in the glass...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2013· Cubist Pharmaceuticals, Inc.

Recalled Item: Cubicin (daptomycin for injection) Recalled by Cubist Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter; Glass particulates observed in vials

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

Class I — Serious Health HazardOngoing
Refund