Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,503 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,503 in last 12 months

Showing 1280112820 of 48,219 recalls

FoodFebruary 17, 2022· Abbott Laboratories

Recalled Item: Abbott Similac Pro-Advance Infant Formula with Iron 20.6oz. and 23.2oz....

The Issue: Consumer complaints related to Cronobacter sakazakii or Salmonella Newport...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 17, 2022· Abbott Laboratories

Recalled Item: Abbott Similac PM 60/40 Low Iron Infant Formula Recalled by Abbott...

The Issue: Consumer complaints related to Cronobacter sakazakii or Salmonella Newport...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 17, 2022· Abbott Laboratories

Recalled Item: Abbott Infant Formula Powder 12.6oz. can. 6 cans per case. Recalled by...

The Issue: Consumer complaints related to Cronobacter sakazakii or Salmonella Newport...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 17, 2022· Abbott Laboratories

Recalled Item: Abbott Similac EleCare HMO Recalled by Abbott Laboratories Due to Potential...

The Issue: Consumer complaints related to Cronobacter sakazakii or Salmonella Newport...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 17, 2022· Abbott Laboratories

Recalled Item: Abbott Similac Alimentum Infant Formula with Iron 12oz. can. 6 jars per case...

The Issue: Consumer complaints related to Cronobacter sakazakii or Salmonella Newport...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 17, 2022· Deerfield Imaging, Inc.

Recalled Item: Trumpf Mount Clamp Assembly (table adapter component) Recalled by Deerfield...

The Issue: Reports have been received that after normal or routine lateral forces are...

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

Class II — Potential Health HazardOngoing
DrugFebruary 16, 2022· TCP HRB ACQUISITON LLC

Recalled Item: Sure Unscented Anti-perspirant Deodorant Aerosol (Aluminum Chlorohydrate...

The Issue: Chemical contamination: Presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 16, 2022· TCP HRB ACQUISITON LLC

Recalled Item: Brut Classic Antiperspirant & Deodorant (aluminum chlorohydrate 20.9%)...

The Issue: Chemical contamination: Presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 16, 2022· TCP HRB ACQUISITON LLC

Recalled Item: Sure Regular Antiperspirant Deodorant Aerosol (Aluminum Chlorohydrate 10%)...

The Issue: Chemical contamination: Presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 16, 2022· Macleods Pharma Usa Inc

Recalled Item: Olanzapine Tablets Recalled by Macleods Pharma Usa Inc Due to cGmp Deviations

The Issue: cGmp Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 16, 2022· Beckman Coulter, Inc.

Recalled Item: Beckman Coulter IRISpec CA/CB/CC control Recalled by Beckman Coulter, Inc....

The Issue: IRISpec CA failures for glucose.

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

Class III — Low RiskOngoing
DrugFebruary 15, 2022· ANI Pharmaceuticals, Inc.

Recalled Item: Pyrazinamide Tablets Recalled by ANI Pharmaceuticals, Inc. Due to cGMP...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2022· Macleods Pharma Usa Inc

Recalled Item: Amlodipine and Olmesartan Medoxomil Tablets Recalled by Macleods Pharma Usa...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2022· ANI Pharmaceuticals, Inc.

Recalled Item: Alprazolam Tablets Recalled by ANI Pharmaceuticals, Inc. Due to cGMP Deviations

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2022· ANI Pharmaceuticals, Inc.

Recalled Item: Alprazolam Tablets Recalled by ANI Pharmaceuticals, Inc. Due to cGMP Deviations

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2022· ANI Pharmaceuticals, Inc.

Recalled Item: Alprazolam Tablets Recalled by ANI Pharmaceuticals, Inc. Due to cGMP Deviations

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2022· ANI Pharmaceuticals, Inc.

Recalled Item: Alprazolam Tablets Recalled by ANI Pharmaceuticals, Inc. Due to cGMP Deviations

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 15, 2022· Meridian Bioscience Inc

Recalled Item: Revogene Recalled by Meridian Bioscience Inc Due to The photomultiplier...

The Issue: The photomultiplier tube, may have compromised functionality in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2022· Draeger Medical, Inc.

Recalled Item: Evita V500 Ventilator with Software 2.51.01 and Lower - intended Recalled by...

The Issue: Cybersecurity Improvement Action-not equipped against potential cyber...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2022· Cook Medical Incorporated

Recalled Item: Gunther Tulip Vena Cava Filter Set for Femoral Vein Approach Recalled by...

The Issue: IFU update includes an update to the Device description, Intended...

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

Class III — Low RiskOngoing