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. 2,431 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,431 in last 12 months

Showing 3870138720 of 49,976 recalls

Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Surgical Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Vaginal Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Vein Kit - No Introducer TVS4027-NI(A convenience custom kits used Recalled...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Custom Venous Kit Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Bayview Abdominoplasty Pack Recalled by Windstone Medical Packaging, Inc....

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Hystero Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: HSG Pack Recalled by Windstone Medical Packaging, Inc. Due to The Medtronic...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Custom Breast Augmentation Pack Recalled by Windstone Medical Packaging,...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Dr Bragg Vein Tray - RX Recalled by Windstone Medical Packaging, Inc. Due to...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Breast Augmentation Pack Recalled by Windstone Medical Packaging, Inc. Due...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Spine Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: Foot Pack Recalled by Windstone Medical Packaging, Inc. Due to The Medtronic...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the...

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

Class II — Potential Health HazardOngoing
DrugApril 21, 2015· Alvogen, Inc

Recalled Item: NITROFURANTOIN MONOHYDRATE/MACROCRYSTALS CAPSULES Recalled by Alvogen, Inc...

The Issue: Failed Dissolution Specification; 6 month time point

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 21, 2015· Spacelabs Healthcare Inc

Recalled Item: Ultraview SL Command Modules Recalled by Spacelabs Healthcare Inc Due to...

The Issue: Modules resetting. This failure mode happens when the Spacelabs Command...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· Stradis Healthcare, LLC.

Recalled Item: Blepharoplasty Pack - contains Devon Light Glove Used during surgery...

The Issue: Convenience kits being recalled due to the recall by the manufacturer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· Stradis Healthcare, LLC.

Recalled Item: Eye Pack - contains Devon Light Glove Used during surgery Recalled by...

The Issue: Convenience kits being recalled due to the recall by the manufacturer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· Stradis Healthcare, LLC.

Recalled Item: Abdominal Pack and Abdom Pack - contains Devon Light Glove Used during...

The Issue: Convenience kits being recalled due to the recall by the manufacturer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· Stradis Healthcare, LLC.

Recalled Item: Head & Neck Pack - contains Devon Light Glove Used during surgery Recalled...

The Issue: Convenience kits being recalled due to the recall by the manufacturer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· ICU Medical, Inc.

Recalled Item: 127" (323cm) Transfer Set w/Check Valve Recalled by ICU Medical, Inc. Due to...

The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2015· Stradis Healthcare, LLC.

Recalled Item: Surgical Pack and General Surgery Pack - contains Devon Light Recalled by...

The Issue: Convenience kits being recalled due to the recall by the manufacturer...

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

Class II — Potential Health HazardOngoing