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. 2,680 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,680 in last 12 months

Showing 26612680 of 28,654 recalls

Medical DeviceNovember 1, 2024· Becton, Dickinson and Company, BD Bio Sciences

Recalled Item: FACSLyric 3L10C Instrument US-IVD Recalled by Becton, Dickinson and Company,...

The Issue: On October 18, 2024, BD has identified through customer complaints and an...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Becton, Dickinson and Company, BD Bio Sciences

Recalled Item: FACSLyric 3L8C Instrument US-IVD Recalled by Becton, Dickinson and Company,...

The Issue: On October 18, 2024, BD has identified through customer complaints and an...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Becton, Dickinson and Company, BD Bio Sciences

Recalled Item: Device Description: FACSLyric 2L6C Instrument US Recalled by Becton,...

The Issue: On October 18, 2024, BD has identified through customer complaints and an...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Cardinal Health 200, LLC

Recalled Item: Convertor Isolation Gown Recalled by Cardinal Health 200, LLC Due to...

The Issue: Isolation Gowns were manufactured with raw materials that may fail the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD EpiCenter Single User Software Version or Model: 441007 Catalog Recalled...

The Issue: BD confirmed that product service credentials used by some BD technical...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190. Model Number:...

The Issue: High-level disinfection ("HLD") with Acecide-C disinfectant in the Olympus...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BACTEC 9240 System Version or Model: 445475 Catalog Number: 445475 Recalled...

The Issue: BD confirmed that product service credentials used by some BD technical...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD COR MX Instrument Version or Model: 443989 Catalog Number: 443989...

The Issue: BD confirmed that product service credentials used by some BD technical...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD EpiCenter Data Management System Version or Model: 440887 Catalog...

The Issue: BD confirmed that product service credentials used by some BD technical...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD COR PX Instrument Version or Model: 443988 Catalog Number: 443988...

The Issue: BD confirmed that product service credentials used by some BD technical...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD BACTEC FX40 Instrument Version or Model: 442296 Catalog Number: 442296...

The Issue: BD confirmed that product service credentials used by some BD technical...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD MAX System Recalled by Becton Dickinson & Co. Due to BD confirmed that...

The Issue: BD confirmed that product service credentials used by some BD technical...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BACTEC 9120 System Version or Model: 445570 Catalog Number: 445570 Recalled...

The Issue: BD confirmed that product service credentials used by some BD technical...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD Phoenix M50 Automated Microbiology System Version or Model: 443624...

The Issue: BD confirmed that product service credentials used by some BD technical...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD COR GX Instrument Version or Model: 443990 Catalog Number: 443990...

The Issue: BD confirmed that product service credentials used by some BD technical...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD BACTEC FX Recalled by Becton Dickinson & Co. Due to BD confirmed that...

The Issue: BD confirmed that product service credentials used by some BD technical...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD Synapsys Informatics Solution (Laboratory Solution) Version or Model:...

The Issue: BD confirmed that product service credentials used by some BD technical...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD EpiCenter Data Management System Recalled by Becton Dickinson & Co. Due...

The Issue: BD confirmed that product service credentials used by some BD technical...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Cartiva, Inc

Recalled Item: Cartiva Synthetic Cartilage Implant (SCI) Catalog: CAR-06-US (6mm) Recalled...

The Issue: Patients implanted with synthetic cartilage implant, may experience a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2024· INCIPIO DEVICES

Recalled Item: Offset Cup Impactor - 3/8-16 interface. Reusable surgical instrument used...

The Issue: Recalled lot does not meet specification and has reported incidents of...

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

Class II — Potential Health HazardOngoing