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. 2,473 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,473 in last 12 months

Showing 1476114780 of 27,884 recalls

Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail 130 Deg 10x165mm Recalled by Zimmer Biomet, Inc....

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF w/AS 550 x 1-14ML/HR 2ML-30LO CPNB Recalled by Arrow International Inc...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Randox Laboratories Ltd.

Recalled Item: Liquid Cardiac Control Recalled by Randox Laboratories Ltd. Due to Randox...

The Issue: Randox has previously issued a recall for Liquid Cardiac Control CQ5053 lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF 550 x 5ML/H 6" DUAL CATHS Recalled by Arrow International Inc Due to...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Pfizer Inc.

Recalled Item: Thermacare Muscle Pain Therapy HeatWraps: a) b) Recalled by Pfizer Inc. Due...

The Issue: The firm received complaints of the wrap coming apart and leaking granular...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 125 Deg 11x300mm Recalled by Zimmer Biomet,...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Pfizer Inc.

Recalled Item: Thermacare HEATWRAPS JOINT PAIN THERAPY Recalled by Pfizer Inc. Due to The...

The Issue: The firm received complaints of the wrap coming apart and leaking granular...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF w/AS 550 x 1-14ML/HR 2ML-15LO CPNB Recalled by Arrow International Inc...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF w/AS 550 x 1-14ML/HR 5ML-60LO CPNB Recalled by Arrow International Inc...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 125 Deg 9x165mm Recalled by Zimmer Biomet,...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF 550 x 5ML/HR CPNB Recalled by Arrow International Inc Due to Possible...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: 0F 550 x 8ML/HR 2ML 60LO CPNB Recalled by Arrow International Inc Due to...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF w/AS 550 x 0.5-7 ml Recalled by Arrow International Inc Due to Possible...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF 550 x 5ML/HR 2ML 60LO CPNB Recalled by Arrow International Inc Due to...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF 550 x 5ML/H 6" CATH Recalled by Arrow International Inc Due to Possible...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF w/AS 550 x 1-14 ml/hr Recalled by Arrow International Inc Due to Possible...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Arrow International Inc

Recalled Item: AF w/AS 550 x 1-14ML/HR CPNB Recalled by Arrow International Inc Due to...

The Issue: Possible cracks on the body of the fill port connector, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Straumann Manufacturing, Inc.

Recalled Item: Neodent¿ GM Mini Conical Abutment - Product Usage: Mini Conical Recalled by...

The Issue: Laser engraved label does not match with the item in the package

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail 130 Deg 12x165mm Recalled by Zimmer Biomet, Inc....

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left Deg 9x300mm Recalled by Zimmer Biomet, Inc....

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing