Product Recalls in Oklahoma
Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,609 recalls have been distributed to Oklahoma in the last 12 months.
Showing 13241–13260 of 49,976 recalls
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.
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.
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.
Recalled Item: LIPOSORBER System Recalled by Kaneka America Corp Due to Labeling change to...
The Issue: Labeling change to due to the risk of severe anaphylactoid reactions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: ProteusPLUS and ProteusONE- designed to produce and deliver a proton...
The Issue: When resuming from a beam pause, the Proton Therapy System does not verify...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
Recalled Item: Cook Celect PlatinumVena Cava Filter Set Catalog Number/GPN:...
The Issue: IFU update includes an update to the Device description, Intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.