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. 2,543 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,543 in last 12 months

Showing 48814900 of 27,884 recalls

Medical DeviceDecember 29, 2023· Philips North America

Recalled Item: Intera 1.5T Recalled by Philips North America Due to An incorrect electrical...

The Issue: An incorrect electrical shock warning label may have been placed on the...

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

Class III — Low RiskOngoing
Medical DeviceDecember 29, 2023· Philips North America

Recalled Item: Achieva 3.0T Recalled by Philips North America Due to An incorrect...

The Issue: An incorrect electrical shock warning label may have been placed on the...

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

Class III — Low RiskOngoing
Medical DeviceDecember 29, 2023· Philips North America

Recalled Item: SmartPath to dStream for 1.5T Recalled by Philips North America Due to An...

The Issue: An incorrect electrical shock warning label may have been placed on the...

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

Class III — Low RiskOngoing
Medical DeviceDecember 29, 2023· Philips North America

Recalled Item: Achieva 1.5T Recalled by Philips North America Due to An incorrect...

The Issue: An incorrect electrical shock warning label may have been placed on the...

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

Class III — Low RiskOngoing
Medical DeviceDecember 29, 2023· Philips North America

Recalled Item: Achieva 1.5T Conversion Recalled by Philips North America Due to An...

The Issue: An incorrect electrical shock warning label may have been placed on the...

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

Class III — Low RiskOngoing
Medical DeviceDecember 29, 2023· Philips North America

Recalled Item: Ingenia Ambition X Recalled by Philips North America Due to An incorrect...

The Issue: An incorrect electrical shock warning label may have been placed on the...

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

Class III — Low RiskOngoing
Medical DeviceDecember 28, 2023· MRP, LLC dba Aquabiliti

Recalled Item: AQUABILITI AQUASTAT 0.9% Sodium Chloride Injection syringe Recalled by MRP,...

The Issue: The saline flush syringes may fail to meet USP criteria for stated sodium...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2023· NeuroLogica Corporation

Recalled Item: Samsung Digital Diagnostic Mobile X-ray System Recalled by NeuroLogica...

The Issue: Mobile x-ray systems moving arm frame welding issue which presents the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6,...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6,...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6,...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6,...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing