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. 2,537 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,537 in last 12 months

Showing 59816000 of 48,376 recalls

Medical DeviceMarch 28, 2024· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 14.0.0.3338. Radiation Therapy Treatment Planning System....

The Issue: Potential for reported SSD to be too high.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2024· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 9.1.0.933 and 9.2.0.483. Radiation Therapy Treatment Planning...

The Issue: Potential for reported SSD to be too high.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2024· Zimmer, Inc.

Recalled Item: NexGen CR-Flex Femoral Component Recalled by Zimmer, Inc. Due to Out of...

The Issue: Out of specification violation of devices that results in a gap existing...

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

Class II — Potential Health HazardOngoing
DrugMarch 27, 2024· Esperion

Recalled Item: NEXLIZET (bempedoic acid and ezetimibe) tablets Recalled by Esperion Due to...

The Issue: Failed dissolution specifications: out-of-specification bempedoic acid...

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

Class III — Low RiskOngoing
Refund
DrugMarch 27, 2024· NATCO Pharma Limited

Recalled Item: Lansoprazole Delayed-Release Capsules USP Recalled by NATCO Pharma Limited...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 27, 2024· Newport Corp

Recalled Item: Newport s N-LHP-928(j) units if sold as a laser head/power supply set...

The Issue: According to 21 CFR 1040.10(f)(4), each laser system classified as a Class...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2024· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt 3-Spring Reservoir with Silicone Adapters Recalled by Cardinal...

The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2024· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain Recalled by...

The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2024· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Universal Connector PVC Tubing Anti Transparent Y Recalled by...

The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2024· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain Recalled by...

The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2024· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain Recalled by...

The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...

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

Class II — Potential Health HazardOngoing
DrugMarch 26, 2024· Cipla USA, Inc.

Recalled Item: Ipratropium Bromide and Albuterol Sulfate Inhalation Solution USP Recalled...

The Issue: Short fill: Complaints received of less fill volume in respule and few drops...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 26, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: Failed Dissolution Specifications: Out of Specification (OOS) was reported...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 26, 2024· Philips Respironics, Inc.

Recalled Item: BiPAP V30 Auto Ventilator Recalled by Philips Respironics, Inc. Due to...

The Issue: Potential for devices to experience interruption/loss of therapy during a...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2024· Philips Respironics, Inc.

Recalled Item: BiPAP A40 Ventilators: BiPAP A40 Recalled by Philips Respironics, Inc. Due...

The Issue: Potential for devices to experience interruption/loss of therapy during a...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2024· Philips Respironics, Inc.

Recalled Item: BiPAP A30 Ventilator Recalled by Philips Respironics, Inc. Due to Potential...

The Issue: Potential for devices to experience interruption/loss of therapy during a...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2024· Medtronic Navigation, Inc.

Recalled Item: Stealth S8 Clinical Software Application Recalled by Medtronic Navigation,...

The Issue: Due to a software issue, there is the potential for a missing digit, letter,...

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

Class I — Serious Health HazardOngoing
DrugMarch 25, 2024· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Methylergonovine Maleate Tablets Recalled by Amneal Pharmaceuticals of New...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2024· Novitium Pharma LLC

Recalled Item: Digoxin Tablets Recalled by Novitium Pharma LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 25, 2024· Ossur H / F

Recalled Item: RKN130002 Recalled by Ossur H / F Due to Due to firmware issues with the...

The Issue: Due to firmware issues with the prosthetic knee, there is the potential for...

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

Class II — Potential Health HazardOngoing