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. 2,353 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,353 in last 12 months

Showing 3086130880 of 48,376 recalls

FoodOctober 20, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Jalapeno Cherry Butter 12oz and 20oz glass bottles Recalled...

The Issue: Products contain milk not declared on the label.

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 20, 2016· Brownwood Farms

Recalled Item: Brownwood Farms America's Original Cherry Butter 12oz and 22oz glass...

The Issue: Products contain milk not declared on the label.

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 20, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Pear & Cinnamon Preserves 10oz glass bottles and 1 gallon....

The Issue: Products contain milk not declared on the label.

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 20, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Strawberry Preserves 12oz glass bottles and 1 gallon....

The Issue: Products contain milk not declared on the label.

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 20, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Cherry Raspberry Preserves 12oz glass bottles and 1 gallon....

The Issue: Products contain milk not declared on the label.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 20, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...

The Issue: Siemens is providing software update version VA50A_SP3 to address the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Recalled by Merge Healthcare, Inc. Due to A product issues happens for...

The Issue: A product issues happens for RF projection images. If user measures on RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2016· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy System Recalled by...

The Issue: Software defect:2D projection of contours in Verity. The defect causes...

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

Class II — Potential Health HazardOngoing
DrugOctober 19, 2016· Janssen Ortho L.L.C.

Recalled Item: Invokamet (canagliflozin and metformin HCl) tablets Recalled by Janssen...

The Issue: Labeling: Incorrect or Missing Package Insert - Xarelto prescribing...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 19, 2016· Greatbatch Medical

Recalled Item: Offset Reamer Handle Recalled by Greatbatch Medical Due to On June 14, 2016,...

The Issue: On June 14, 2016, Greatbatch discovered a significant increase in the number...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Beckman Coulter Inc.

Recalled Item: AQUIOS Lyse Reagent Kit Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is recalling the AQUIOS Lyse Reagent Kit because it may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: A problem can occur with the small light marker windows, used for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur CA 19-9 Assay (50 test kit)-for use Recalled by Siemens...

The Issue: CA 19-9 assay on the ADVIA Centaur CP does not meet the correlation to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur CA 19-9 Assay (250 test kit)-for use Recalled by Siemens...

The Issue: CA 19-9 assay on the ADVIA Centaur CP does not meet the correlation to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: A problem can occur with the small light marker windows, used for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS system Recalled by Siemens Medical Solutions USA, Inc...

The Issue: Hardware issue that may expose the User to a potential risk for serious...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash system Recalled by Siemens Medical Solutions USA,...

The Issue: Hardware issue that may expose the user to a potential risk for serious...

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

Class II — Potential Health HazardOngoing
DrugOctober 18, 2016· Town and Country Compounding and Consultation Services, LLC

Recalled Item: HCG (Chorionic Gonadotropin Lyopholized) II Recalled by Town and Country...

The Issue: Subpotent Drug: due to failed potency results of 74% (spec. 80-125%).

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

Class III — Low RiskOngoing
Refund
DrugOctober 18, 2016· GSK Consumer Healthcare

Recalled Item: Zeasorb AF (miconazole nitrate) Recalled by GSK Consumer Healthcare Due to...

The Issue: Labeling Not Elsewhere Classified: front labels have the incorrect NDC or...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 18, 2016· Teleflex Medical

Recalled Item: Sheridan/CF Recalled by Teleflex Medical Due to Labeling inconsistency -...

The Issue: Labeling inconsistency - units labeled with a 7mm tube may contain a size...

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

Class II — Potential Health HazardOngoing