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. 2,521 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,521 in last 12 months

Showing 1030110320 of 48,376 recalls

Medical DeviceNovember 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Luminos dRF Max (VE10 Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Under certain unlikely circumstances during a fluoroscopic examination, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: LUMINOS Lotus Max (VF11) Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Under certain unlikely circumstances during a fluoroscopic examination, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2022· Baxter Healthcare Corporation

Recalled Item: Revaclear 300 dialyzers. Indicated for treatment of chronic and acute...

The Issue: Reports of Polyurethane Displacement in the dialyzer, and might be...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2022· Baxter Healthcare Corporation

Recalled Item: Revaclear 400 dialyzers. Indicated for treatment of chronic and acute...

The Issue: Reports of Polyurethane Displacement in the dialyzer, and might be...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2022· Baxter Healthcare Corporation

Recalled Item: Revaclear 400 Dialyzer. Product Code: 114749M. Not distributed in the...

The Issue: Potential for Internal Blood Leaks due to a twisted gasket in the dialyzer

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2022· Baxter Healthcare Corporation

Recalled Item: Revaclear 400 Dialyzer. Product Code: 114746L. Used to treat chronic...

The Issue: Potential for Internal Blood Leaks due to a twisted gasket in the dialyzer

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2022· Baxter Healthcare Corporation

Recalled Item: Revaclear 400 dialyzers. Indicated for treatment of chronic and acute...

The Issue: Reports of Polyurethane Displacement in the dialyzer, and might be...

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

Class II — Potential Health HazardOngoing
DrugNovember 22, 2022· Fresenius Kabi USA, LLC

Recalled Item: Sensorcaine (Bupivacaine HCl and Epinephrine Injection Recalled by Fresenius...

The Issue: Subpotent Drug: Testing results below the defined limit for the epinephrine...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 22, 2022· Fresenius Kabi USA, LLC

Recalled Item: Sensorcaine-MPF (Bupivacaine HCl and Epinephrine Injection Recalled by...

The Issue: Subpotent Drug: Testing results below the defined limit for the epinephrine...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 22, 2022· Fresenius Kabi USA, LLC

Recalled Item: Sensorcaine (Bupivacaine HCl and Epinephrine Injection Recalled by Fresenius...

The Issue: Subpotent Drug: Testing results below the defined limit for the epinephrine...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 22, 2022· Fresenius Medical Care Holdings, Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Fresenius Medical Care Holdings,...

The Issue: Lack of Assurance of Sterility: Leakage of 0.9% Sodium Chloride for...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 22, 2022· XO Marshmallow, LLC

Recalled Item: XO Marshmallow Limited Edition: Banana Puddin' OMG (Ooey Marshmallow...

The Issue: No label on packaged product

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 22, 2022· Randox Laboratories Ltd.

Recalled Item: Liquid Assayed Specific Protein Control Level 2- In vitro diagnostic use...

The Issue: Concentration of Rheumatoid Factor has decreased in Specific Protein Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Randox Laboratories Ltd.

Recalled Item: Liquid Assayed Specific Protein- In vitro diagnostic use Recalled by Randox...

The Issue: Concentration of Rheumatoid Factor has decreased in Specific Protein Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Randox Laboratories Ltd.

Recalled Item: Liquid Assayed Specific Protein Control Level 3- In vitro diagnostic use...

The Issue: Concentration of Rheumatoid Factor has decreased in Specific Protein Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Philips North America Llc

Recalled Item: Philips SmartPath to Ingenia Elition X MR System Recalled by Philips North...

The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Philips North America Llc

Recalled Item: Philips MR 7700 System Recalled by Philips North America Llc Due to Gradient...

The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Philips North America Llc

Recalled Item: Philips Ingenia Elition S MR System Recalled by Philips North America Llc...

The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Philips North America Llc

Recalled Item: Philips Ingenia Elition X MR System Recalled by Philips North America Llc...

The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2022· Philips North America Llc

Recalled Item: Philips Upgrade to MR 7700 System Recalled by Philips North America Llc Due...

The Issue: Gradient Coil may act as a heat source with a potential to produce smoke...

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

Class II — Potential Health HazardOngoing