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. 1,030 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
1,030 in last 12 months

Showing 20381–20400 of 49,976 recalls

Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Haemonetics Corporation

Recalled Item: CS Elite Processing Set (225 ml) Autotransfusion Device - Product Recalled...

The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Integra LifeSciences Corp.

Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...

The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Integra LifeSciences Corp.

Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...

The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Haemonetics Corporation

Recalled Item: Japan CS Elite FASTPACK DISP. SET - 125ML - Product Recalled by Haemonetics...

The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Integra LifeSciences Corp.

Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...

The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Integra LifeSciences Corp.

Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...

The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Integra LifeSciences Corp.

Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...

The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
DrugOctober 21, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: PF-Succinylcholine Chloride Injection Recalled by Nephron Pharmaceuticals...

The Issue: Incorrect labeling: Incorrect or missing lot and/or exp date

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 21, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-96 plus Instrument Recalled by Beckman Coulter Inc. Due...

The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Beckman Coulter Inc.

Recalled Item: DxM 1040 MicroScan WalkAway Instrument Recalled by Beckman Coulter Inc. Due...

The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-96 plus Reconditioned Instrument Recalled by Beckman...

The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...

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

Class II — Potential Health HazardOngoing