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. 910 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
910 in last 12 months

Showing 52101–52120 of 54,363 recalls

Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Vital Signs Devices, a GE Healthcare Company

Recalled Item: Corometrics Qwik Connect Plus Spiral Electrode- Model #7000AA0 A fetal...

The Issue: Thirty fetal scalp electrodes were found to have an incomplete package seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux BacT/ALERT Combo Module Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux BacT/ALERT Control Module Recalled by Biomerieux Inc Due to...

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux BacT/ALERT Combo Module Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux BacT/ALERT Control Module Recalled by Biomerieux Inc Due to...

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing