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. 2,345 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,345 in last 12 months

Showing 3210132120 of 48,376 recalls

Medical DeviceJuly 6, 2016· Bard Peripheral Vascular Inc

Recalled Item: Bard TruGuide Disposable Coaxial Biopsy Needle  Mixed Product Part Recalled...

The Issue: May contain two trocar tip stylets with coaxials or two blunt tip stylets...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2016· Smith & Nephew, Inc.

Recalled Item: SPHERICAL HEAD (R) 6.5 MM CANCELLOUS SCREW Recalled by Smith & Nephew, Inc....

The Issue: The labels correctly state that the product should be a 25mm screw, but the...

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

Class II — Potential Health HazardOngoing
DrugJuly 5, 2016· Let's Talk Health, Inc.

Recalled Item: Oxygen Nasal Wash (purified water Recalled by Let's Talk Health, Inc. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: product is an unapproved drug due to...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 5, 2016· Newly Weds Foods Inc

Recalled Item: Bulk flour bland breader packaged into 15 Recalled by Newly Weds Foods Inc...

The Issue: Flour contaminated with E. coli O121 was used in the manufacuring of flour...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 5, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint¿ 500 v2.2.2A Software Upgrade Kit Recalled by Siemens...

The Issue: Some v2.2.2 upgrade kits include a dialysate mode which not cleared/approved...

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

Class III — Low RiskOngoing
Medical DeviceJuly 5, 2016· Branan Medical Corporation

Recalled Item: AmediCheck Instant Test Cup Recalled by Branan Medical Corporation Due to...

The Issue: Branan Medical is recalling the AmediCheck Instant Test Cup, a 5 panel drug...

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

Class III — Low RiskOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Handpiece Loaner Recalled by Zimmer Surgical Inc...

The Issue: Zimmer Biomet Surgical has received product complaints reporting that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Handpiece w/o Hose Recalled by Zimmer Surgical Inc...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Handpiece Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2016· Circulatory Technology Inc

Recalled Item: The Better-Bladder With 14" ID tubing Recalled by Circulatory Technology Inc...

The Issue: Twisted or wrinkled balloon components which are considered a cosmetic...

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

Class III — Low RiskOngoing
Medical DeviceJuly 1, 2016· Sysmex America Inc

Recalled Item: Fluorocell PLT reagent Recalled by Sysmex America Inc Due to There is a...

The Issue: There is a potential that fluorescent platelet (PLT-F) and immature platelet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2016· Nidek Inc

Recalled Item: OPTICAL BIOMETER AL-Scan: Software Version: 1.09 and earlier. Ophthalmic:...

The Issue: Nidek Inc. received information from our manufacturer NIDEK CO. Japan that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Orthopedic manual surgical instrument Usage: Exeter Rasp Handle is a...

The Issue: Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle.

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

Class II — Potential Health HazardOngoing
DrugJune 30, 2016· Allergan Sales, LLC

Recalled Item: TAZORAC (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...

The Issue: Failed Content Uniformity Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 30, 2016· Allergan Sales, LLC

Recalled Item: TAZORAC (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...

The Issue: Failed Content Uniformity Specifications

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

Class II — Potential Health HazardOngoing
Refund