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. 1,924 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,924 in last 12 months

Showing 2056120580 of 29,737 recalls

Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: MACH AxiEM Cranial Treon. The software application is sent in Recalled by...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-330BR Bovie Precise 360 Handpiece 33cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: FrameLink. The software application is sent in CD format with an IFU...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: S7 MACH FrameLink. The software application is sent in CD format with an IFU...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Aribex Inc

Recalled Item: NOMAD Pro Packaged X-Ray System Recalled by Aribex Inc Due to Firm received...

The Issue: Firm received customer complaints where end users reported that Nomad Pro...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Cepheid

Recalled Item: Xpert MRSA Catalog GXMRSA-120 Recalled by Cepheid Due to Internal...

The Issue: Internal investigation found the certain lots of MRSA kits have the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: Synergy Spine. The software application is sent in CD format with an IFU...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: Synergy Cranial S7. The software application is sent in CD format with an...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-330NR Bovie Precise 360 Handpiece 33cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Hill-Rom, Inc.

Recalled Item: Affinity Four Birthing Bed Model P3700 The primary packaging is Recalled by...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Modular Pre Analytics ( EVO/Plus) Product Usage: The RSD 800A Recalled by...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Roche COBAS INTEGRA 800 /800 CTS Analyzer Analyzer Recalled by Roche...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Topcon Medical Laser Systems, Inc

Recalled Item: Opthalmic: PASCAL Synthesis is an ophthalmic scanning laser system. The...

The Issue: Topcon discovered an anomaly with titration, only when EpM is turned on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas 6000 Series system c6000 Recalled by Roche Diagnostics Operations,...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas e411 Immunoassay Analyzer e411: Immunoassay Analyzer Product Usage:...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: RSD 800A Aliquoting System calculator/data processing module Recalled by...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas p 612 Pre-Analytical Instrument calculator/data processing module...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System Recalled by Elekta, Inc. Due to It is...

The Issue: It is possible that a change to an Order Set will not be saved in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas p 512 Pre-Analytical Instrument calculator/data processing module...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas p 501 Post-Analytical Unit calculator/data processing module Recalled...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing