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. 1,098 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,098 in last 12 months

Showing 11881–11900 of 29,737 recalls

Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 6 Service Pack 2 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 8A Service Pack 1 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 8B Service Pack 2 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 8B Service Pack 1 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: PHANTOM CS DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· Mediana Co., Ltd.

Recalled Item: DIRECT SUPPLY Attendant VITAL SIGNS MONITOR Recalled by Mediana Co., Ltd....

The Issue: Failures were found in the temperature measurement function while in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: (1) Atellica Data Manager software version 1.0 Siemens Material Number...

The Issue: Unexpected interface driver behavior identified (QC) Results May Be Assigned...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: (1) CentraLink Data Management System software version 16.0.2 Siemens...

The Issue: Unexpected interface driver behavior identified (QC) Results May Be Assigned...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· Siemens Healthcare Diagnostics Inc.

Recalled Item: Siemens IMMULITE 2000 Immunoassay System - In vitro Chemistry Analyzer...

The Issue: Flexible tubing connected to the liquid waste bottle can crack during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: 3COR DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due to...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: PHANTOM CS QUICK START DISTRACTION SCREW Recalled by TeDan Surgical...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: PHANTOM CS QUICK START DISTRACTION SCREW Recalled by TeDan Surgical...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: PHANTOM CS QUICK START DISTRACTION SCREW Recalled by TeDan Surgical...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· Siemens Healthcare Diagnostics Inc.

Recalled Item: Siemens IMMULITE 2000 XPi Immunoassay System - In vitro Chemistry Recalled...

The Issue: Flexible tubing connected to the liquid waste bottle can crack during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: PHANTOM CS DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: 3COR DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due to...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE LEFT 11 HOLE 197MM...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Bound Tree Medical

Recalled Item: Curaplex Ambu King LTS-D Supraglottic Airway Kit with ET Tube Recalled by...

The Issue: Kit contained an incorrect catheter-tip syringe not compatible with the luer...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S.¿ PROXIMAL HUMERUS PLATING SYSTEM PROXIMAL HUMERUS PLATE TEMPLATE...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM DRILL BLOCK SET SCREW Recalled by...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing