Product Recalls in North Carolina

Product recalls affecting North Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to North Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,920 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,920 in last 12 months

Showing 2342123440 of 29,737 recalls

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

Recalled Item: Head and Neck 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: Transvaginal 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: 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
Medical DeviceApril 22, 2015· Windstone Medical Packaging, Inc.

Recalled Item: General Male 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: Morris Hysto 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 21, 2015· Zimmer Surgical Inc

Recalled Item: Zimmer 100 mL Hemovac Device Hemovac Mini Evacuator. 00-2568-000-10. Zimmer...

The Issue: Devices were placed in a shipper carton without the appropriate number of...

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

Class III — Low RiskOngoing
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: Knee Arthro Pack and Knee Arthro Pack II - contains Recalled by Stradis...

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· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Emotion 16 Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Software bugs in VC20B SP0a or SP1 software versions may cause issues that...

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: Set Up 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: Bariatric 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: Orthopedic Split Drape 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: Glaucoma 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: Neurosurgery 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· Stradis Healthcare, LLC.

Recalled Item: Gyn 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: 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: Suction 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: Breast Augmentation Pack and Breast Augmentation Expanded Pack - contains...

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