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. 1,932 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,932 in last 12 months

Showing 2012120140 of 29,737 recalls

Medical DeviceSeptember 29, 2016· Mako Surgical Corporation

Recalled Item: Stryker Restoris RIO Reamer Handle Recalled by Mako Surgical Corporation Due...

The Issue: Failure of the Offset Cup Reamer Handle not engaging its mating components.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· Thayer Medical Corporation

Recalled Item: Thayer MiniSpacer Dual Spray MDI Adapter Counter Incrementing Actuator with...

The Issue: The insert and case label description of the device incorrectly reads...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· Sorin Group USA, Inc.

Recalled Item: The ORCHESTRA Programmer A portable device Recalled by Sorin Group USA, Inc....

The Issue: Sorin Group USA, Inc. announces a voluntary field action for the ORCHESTRA...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· Nonin Medical, Inc

Recalled Item: 8500M Handheld Pulse Oximeter Recalled by Nonin Medical, Inc Due to Nonin...

The Issue: Nonin manufactures and sells two 8500 handheld pulse oximeters (Model 8500...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: FlexLab Automation Modules Recalled by Siemens Healthcare Diagnostics, Inc....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· Covidien LLC

Recalled Item: Professional Hospital Supply Recalled by Covidien LLC Due to Added...

The Issue: Added Instructions for Use: After application, inspect the Light Glove for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· Covidien LLC

Recalled Item: Covidien Devon Light Glove packaged in sterile surgical kits : Recalled by...

The Issue: Added Instructions for Use: After application, inspect the Light Glove for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2016· Covidien LLC

Recalled Item: Covidien Devon Light Glove sub-assembly non-sterile For Kit Packers Product...

The Issue: Added Instructions for Use: After application, inspect the Light Glove for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS 4F Stiffened Micro-Introducer Recalled by Angiodynamics, Inc....

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Baxter Healthcare Corp.

Recalled Item: Baxter SIGMA Spectrum INFUSION PUMP with Master Drug Library Recalled by...

The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Baxter Healthcare Corp.

Recalled Item: sigma spectrum VOLUMETRIC INFUSION PUMP with Master Drug Library Recalled by...

The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Baxter Healthcare Corp.

Recalled Item: V6 Rear Case Assembly Recalled by Baxter Healthcare Corp. Due to A...

The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Zimmer Biomet, Inc.

Recalled Item: Zimmer¿ Gender Solutions" Patellofemoral Joint Prosthesis Milling Handpiece...

The Issue: Complaints have been reported that the handpiece is inoperable. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: Transpac¿ IV Monitoring Kit w/ Safeset" Reservoir and Blood Sampling Port...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing