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. 2,647 recalls have been distributed to Oklahoma in the last 12 months.
Showing 6841–6860 of 49,976 recalls
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custodiol HTK Solution Recalled by Dr Franz Koehler Chemie Gmbh Due to...
The Issue: Potential for particles to be present in solution.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Invos Recalled by Covidien Due to manufacturing defects to sensor...
The Issue: manufacturing defects to sensor cable connectors may result in error codes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Invos Recalled by Covidien Due to manufacturing defects to sensor...
The Issue: manufacturing defects to sensor cable connectors may result in error codes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST" Recalled by...
The Issue: Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sekisui Diagnostics Control Kit OSOM¿ BVBLUE¿ Bacterial Vaginosis Recalled...
The Issue: Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Point of Care Control Control i-STAT¿ Level 1 10 X 1.7 mL Recalled by...
The Issue: Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Rapid Dx N America LLC Reproductive Endocrinology Control Set...
The Issue: Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Point of Care Control Control i-STAT¿ Level 3 1.7 mL Recalled by...
The Issue: Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DISP.HASSON TROCAR 10/110MM Recalled by Aesculap Inc Due to The sterile...
The Issue: The sterile blister packaging may be damaged, and sterility may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DISP.TROCAR W.DILATING PIN 12/110MM Recalled by Aesculap Inc Due to The...
The Issue: The sterile blister packaging may be damaged, and sterility may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DISP.TROCAR W.DILATING PIN 12/110MM Recalled by Aesculap Inc Due to The...
The Issue: The sterile blister packaging may be damaged, and sterility may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DISP.TROCAR W. DILATING PIN 10/110MM Recalled by Aesculap Inc Due to The...
The Issue: The sterile blister packaging may be damaged, and sterility may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DISP.HASSON TROCAR 12/110MM Recalled by Aesculap Inc Due to The sterile...
The Issue: The sterile blister packaging may be damaged, and sterility may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: the original BENNY T'S VESTA DRY HOT SAUCE SCORPION NWT Recalled by Benny Ts...
The Issue: The firm was notified by the North Carolina Dept of Agriculture and Consumer...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: the original BENNY T'S VESTA DRY HOT SAUCE HOT NET Recalled by Benny Ts...
The Issue: The firm was notified by the North Carolina Dept of Agriculture and Consumer...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: the original BENNY T'S VESTA DRY HOT SAUCE REAPER NET Recalled by Benny Ts...
The Issue: The firm was notified by the North Carolina Dept of Agriculture and Consumer...
Recommended Action: Do not consume. Return to store for a refund or discard.