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. 1,887 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,887 in last 12 months

Showing 2900129020 of 29,737 recalls

Medical DeviceJune 18, 2012· Hill-Rom, Inc.

Recalled Item: Advanta 2 Bed. The Advanta 2 Bed is intended for Recalled by Hill-Rom, Inc....

The Issue: During an evaluation of Advanta 2 siderail samples returned from the field...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· superDimension, Inc

Recalled Item: superDimension Systems AAS00016-xx with Software Version 4.0-4.9. Indicated...

The Issue: superDimension, Inc., is conducting a recall of certain superDimension...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Cardiovascular Systems, Inc.

Recalled Item: CSI Stealth 360-degree Orbital Atherectomy Device (OAD) Recalled by...

The Issue: CSI has initiated a recall on specific lot numbers of Stealth 360-degree...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1. System 1 base 100/120V. The Recalled by...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 9000 Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1. System 1 base 220/240V. The Recalled by...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Varian Medical Systems, Inc. Oncology Systems

Recalled Item: Varian brand Varian Eclipse Treatment Planning System for radiotherapy...

The Issue: Varian has identified an anomaly with the Eclipse Treatment Planning (for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 9000 Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 9000 Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2012· DeRoyal Industries Inc

Recalled Item: Custom surgical kits and trays: GEO-MED TOTAL KNEE PACK PGYBK Recalled by...

The Issue: Surgical kits and trays contain Stryker Hytrel Togas which were recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Equinoxe Reverse Shoulder Fracture Adapter Tray Screw Intended for Primary...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Diagnostica Stago, Inc.

Recalled Item: STA Satellite Automated Multi-Parameter Analyzer This system is a fully...

The Issue: Following a single customer complaint that incorrect INR values were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Equinoxe Anatomic Replicator Plate Intended for Primary and Reverse Total...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Hitachi Medical Systems America Inc

Recalled Item: Hitachi Echelon MRI System/Oasis MRI Recalled by Hitachi Medical Systems...

The Issue: Hitachi discovered a software error with a feature called Multi-Planar...

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

Class II — Potential Health HazardOngoing