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. 2,801 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
2,801 in last 12 months

Showing 55815600 of 29,737 recalls

Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: DigitalDiagnost 4 Chest/Emergency Recalled by Philips North America Llc Due...

The Issue: Potential for units suspended on the ceiling to fail and fall.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: CombiDiagnost R90 Recalled by Philips North America Llc Due to Potential for...

The Issue: Potential for units suspended on the ceiling to fail and fall.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: DigitalDiagnost 4 High Performance Recalled by Philips North America Llc Due...

The Issue: Potential for units suspended on the ceiling to fail and fall.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: DigitalDiagnost C90 Release 3 Recalled by Philips North America Llc Due to...

The Issue: Potential for units suspended on the ceiling to fail and fall.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: DigitalDiagnost C90 Release 3.1 Recalled by Philips North America Llc Due to...

The Issue: Potential for units suspended on the ceiling to fail and fall.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: ProxiDiagnost N90 Recalled by Philips North America Llc Due to Potential for...

The Issue: Potential for units suspended on the ceiling to fail and fall.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: DigitalDiagnost C90 High Performance Recalled by Philips North America Llc...

The Issue: Potential for units suspended on the ceiling to fail and fall.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: DigitalDiagnost C90 Flex/Value/Chest/ER Recalled by Philips North America...

The Issue: Potential for units suspended on the ceiling to fail and fall.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: EasyDiagnost Eleva DRF Recalled by Philips North America Llc Due to...

The Issue: Potential for units suspended on the ceiling to fail and fall.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: DigitalDiagnost 4 Flex/Value Recalled by Philips North America Llc Due to...

The Issue: Potential for units suspended on the ceiling to fail and fall.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· B. Braun Medical, Inc.

Recalled Item: 8713051U Recalled by B. Braun Medical, Inc. Due to Upstream occlusion alarm...

The Issue: Upstream occlusion alarm may sound when no occlusion exists, and the device...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 21, 2023· B. Braun Medical, Inc.

Recalled Item: 8713052U Recalled by B. Braun Medical, Inc. Due to Upstream occlusion alarm...

The Issue: Upstream occlusion alarm may sound when no occlusion exists, and the device...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 21, 2023· Acclarent, Inc.

Recalled Item: TruDi Navigation System Recalled by Acclarent, Inc. Due to When using...

The Issue: When using affected curette and software, there is a discrepancy between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2023· Cardinal Health 200, LLC

Recalled Item: Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack Recalled by...

The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2023· Cardinal Health 200, LLC

Recalled Item: Monoject 20 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...

The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2023· Cardinal Health 200, LLC

Recalled Item: Monoject" 60 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...

The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2023· Cardinal Health 200, LLC

Recalled Item: Monoject" 12 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...

The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2023· Cardinal Health 200, LLC

Recalled Item: Monoject" 6 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...

The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2023· Cardinal Health 200, LLC

Recalled Item: Monoject" 35 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...

The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2023· NeuroSync, Inc.

Recalled Item: NeuroSync EYE-SYNC containing Pico Neo 2 Headsets. Each unit consists...

The Issue: Eye syncing issues causing the device to be inoperable. Unable to be...

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

Class II — Potential Health HazardOngoing