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. 2,431 recalls have been distributed to Oklahoma in the last 12 months.
Showing 38801–38820 of 49,976 recalls
Recalled Item: Surgical Set Up kit Recalled by Covidien LLC Due to Devon Light Gloves...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Recalled by Biomet, Inc. Due to Biomet hip...
The Issue: Biomet hip joint, knee joint and shoulder joint replacement components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Cobalt-Chrome Femoral Components Recalled by Biomet, Inc. Due to...
The Issue: Biomet hip joint, knee joint and shoulder joint replacement components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mallory/Head Primary Hip System Recalled by Biomet, Inc. Due to Biomet hip...
The Issue: Biomet hip joint, knee joint and shoulder joint replacement components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MCK Maximum Congruent Knee System Recalled by Biomet, Inc. Due to Biomet hip...
The Issue: Biomet hip joint, knee joint and shoulder joint replacement components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....
The Issue: The term DORSAL was laser etched on the incorrect side on some of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....
The Issue: The term DORSAL was laser etched on the incorrect side on some of the angled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....
The Issue: The term DORSAL was laser etched on the incorrect side on some of the angled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....
The Issue: The term DORSAL was laser etched on the incorrect side on some of the angled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tapered HD Upgrade Set Recalled by BioHorizons Implant Systems Inc Due to...
The Issue: BioHorizons Tapered HD Upgrade set was packaged with an incorrect drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Oasis MRI System Recalled by Hitachi Medical Systems America Inc Due...
The Issue: Image data transferred from the MRI system to a workstation showed errors on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Echelon MRI System Recalled by Hitachi Medical Systems America Inc...
The Issue: Image data transferred from the MRI system to a workstation showed errors on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Echelon Oval MRI System Recalled by Hitachi Medical Systems America...
The Issue: Image data transferred from the MRI system to a workstation showed errors on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Well at Walgreens Maximum Strength Comfort Gel 12 FL OZ (355 mL) bottle...
The Issue: Products failed the Antimicrobial Effectiveness Test
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Well at Walgreens Regular Strength Antacid Liquid Recalled by Tarmac...
The Issue: Products failed the Antimicrobial Effectiveness Test.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Well at Walgreens Regular Strength Comfort Gel Cherry Flavor Recalled by...
The Issue: Products failed the Antimicrobial Effectiveness Test
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cetirizine HCl Chewable Tablet Recalled by Sandoz, Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: An out of specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mucinex Fast Max DM Max Recalled by Reckitt Benckiser LLC Due to Labeling:...
The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mucinex Fast Max Day Time Severe Cold and Fast-Max Night Recalled by Reckitt...
The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mucinex Fast Max Day Time Severe Congestion & Cough Night Time Cold & Flu...
The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.