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. 2,660 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,660 in last 12 months

Showing 48414860 of 28,654 recalls

Medical DeviceJanuary 9, 2024· Mckesson Medical-Surgical Inc. Corporate Office

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Mckesson Medical-Surgical Inc. Corporate Office

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Mckesson Medical-Surgical Inc. Corporate Office

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Aesculap Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Aesculap Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Aesculap Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Aesculap Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Aesculap Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Microbiologics Inc

Recalled Item: Microbiologics Enteric Pathogens Control Panel (Inactivated Pellet) Recalled...

The Issue: The negative control was contaminated with one of the positive control...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Piperacillin/Tazobactam- 100/10 ug Recalled by Becton...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Azithromycin -15 ¿g Recalled by Becton Dickinson & Co. Due...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Rifampin- 5 ug Recalled by Becton Dickinson & Co. Due to...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Cefpodoxime - 10 ug Recalled by Becton Dickinson & Co. Due...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: Sensi Disc Amoxicillin with Clavulanic Acid 20/10 ¿g Recalled by Becton...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Minocycline - 30 ug Recalled by Becton Dickinson & Co. Due...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Cefaclor - 30 ug¿ Recalled by Becton Dickinson & Co. Due...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Cefotaxime - 30 ug¿ Recalled by Becton Dickinson & Co. Due...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Tetracycline 30 ug Recalled by Becton Dickinson & Co. Due...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Meropenem- 10 ug Recalled by Becton Dickinson & Co. Due to...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Ceftaroline - 30 ug Recalled by Becton Dickinson & Co. Due...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing