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. 1,790 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
1,790 in last 12 months

Showing 2588125900 of 48,376 recalls

Medical DeviceMarch 12, 2018· CooperSurgical, Inc.

Recalled Item: 5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length...

The Issue: Products have been packaged with the wrong Trocar length type.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Stryker GmbH

Recalled Item: Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation...

The Issue: The wrong parts were picked for packaging. The connecting Nuts were packed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: Power-LOAD Cot Fastening System Recalled by Stryker Medical Division of...

The Issue: The power load floor plates which hold the ambulance cot anchors in place...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Zimmer Biomet, Inc.

Recalled Item: Phoenix Nail System Recalled by Zimmer Biomet, Inc. Due to Certain lots of...

The Issue: Certain lots of the Phoenix Tibia Nail 3.5mm Inserter instruments are being...

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

Class II — Potential Health HazardOngoing
DrugMarch 9, 2018· Akorn, Inc.

Recalled Item: Triamcinolone Acetonide Lotion Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

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

Class III — Low RiskOngoing
Refund
DrugMarch 9, 2018· Alva-Amco Pharmacal Companies., Inc.

Recalled Item: Psoriasin Daytime Relief Cream with Vitamin D & Oatmeal Recalled by...

The Issue: Subpotent Drug: The product has failed to maintain its label claim of coal...

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

Class III — Low RiskOngoing
Refund
DrugMarch 8, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Clocortolone Pivalate Cream Recalled by Dr. Reddy's Laboratories, Inc. Due...

The Issue: Failed Stability Specifications:Out-of-specification results observed for...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Oxytocin USP Recalled by American Pharmaceutical Ingredients LLC Due to...

The Issue: Stability Data Does Not Support Expiry: Stability data from manufacturer...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Sermorelin Acetate Recalled by American Pharmaceutical Ingredients LLC Due...

The Issue: Stability Data Does Not Support Expiry: Stability data from manufacturer...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences EZ Glide Aortic Cannula Recalled by SPS Sterilization,...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Femoral Venous Cannula Recalled by SPS Sterilization,...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Thin-Flex Single Stage Venous Drainage Cannula Recalled...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Avid Dual Stage Venous Drainage Cannula Recalled by SPS...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Thin-Flex Single Stage Venous Drainage Cannula Recalled...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Aortic Perfusion Cannula Recalled by SPS Sterilization,...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Boston Scientific Wallstent Endoprosthesis Tracheobronchial Transhepatic...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Boston Scientific Wallstent Enteral Endoprosthesis Colonic/Duodenal Stent...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial Transhepatic...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Vascular Solutions Venture Rx Catheter Recalled by SPS Sterilization, Inc...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing