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 25612580 of 28,654 recalls

Medical DeviceNovember 19, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8)...

The Issue: Devices were identified as released after repair without full testing being...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)...

The Issue: Devices were identified as released after repair without full testing being...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2024· Olympus Corporation of the Americas

Recalled Item: Duravent Silicone Ventilation Tube. Model Number: 240075. Recalled by...

The Issue: Potential that Duravent Silicone Ventilation Tubes may contain incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) CENTRAL LINE DRESSING KIT Recalled by...

The Issue: Certain Medline kits were manufactured and distributed with Procedure Masks...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) Port Access Kit Recalled by MEDLINE...

The Issue: Certain Medline kits were manufactured and distributed with Procedure Masks...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) SHORT TERM INFUSAPORT ACCESS KIT...

The Issue: Certain Medline kits were manufactured and distributed with Procedure Masks...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2024· GE Medical Systems, LLC

Recalled Item: Tec 820 ISO Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...

The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2024· GE Medical Systems, LLC

Recalled Item: Tec 850 SEV Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...

The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2024· GE Medical Systems, LLC

Recalled Item: Tec 6 Plus Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...

The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2024· GE Medical Systems, LLC

Recalled Item: Tec 850 ISO Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...

The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2024· GE Medical Systems, LLC

Recalled Item: Tec 820 SEV Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...

The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2024· Philips North America Llc

Recalled Item: Spectral CT and Spectral CT Plus. Model Numbers: 728333 Recalled by Philips...

The Issue: Potential for a plan box not updated issue during Interventional procedure...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2024· Mint Medical GmbH

Recalled Item: mint Lesion Recalled by Mint Medical GmbH Due to Some software versions have...

The Issue: Some software versions have a malfunction where they may show incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2024· Mint Medical GmbH

Recalled Item: mint Lesion Recalled by Mint Medical GmbH Due to Some software versions have...

The Issue: Some software versions have a malfunction where they may show incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2024· Kirwan Surgical Products, LLC

Recalled Item: Optikon Bipolar Pencil 25 Gauge Straight. Model/Catalog Number: OPT14-5011....

The Issue: Potential for the outer stainless-steel tube to break or detach.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 14, 2024· Kirwan Surgical Products, LLC

Recalled Item: Walcott Bipolar Pencil 25 Gauge Straight. Model/Catalog Number: RX14-5011....

The Issue: Potential for the outer stainless-steel tube to break or detach.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 14, 2024· Kirwan Surgical Products, LLC

Recalled Item: Kirwan Surgical Products LLC Disposable 25-gauge bipolar pencil Recalled by...

The Issue: Potential for the outer stainless-steel tube to break or detach.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 14, 2024· Kirwan Surgical Products, LLC

Recalled Item: Ambler Surgical Bipolar Pencil 25 Gauge Straight. Model/Catalog Number:...

The Issue: Potential for the outer stainless-steel tube to break or detach.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 14, 2024· Kirwan Surgical Products, LLC

Recalled Item: Nidek Co. Disposable Bipolar Pencil 25 Gauge Straight. Model/Catalog Number:...

The Issue: Potential for the outer stainless-steel tube to break or detach.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 14, 2024· Kirwan Surgical Products, LLC

Recalled Item: Accutome/Microsurgical Disposable Bipolar Pencil 5 in. (12.7cm) 25 Gauge...

The Issue: Potential for the outer stainless-steel tube to break or detach.

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

Class I — Serious Health HazardOngoing