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. 2,789 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
2,789 in last 12 months

Showing 79217940 of 29,737 recalls

Medical DeviceJuly 21, 2022· Cardiac Assist, Inc

Recalled Item: TANDEM LIFE LivaNova LIFESPARC Controller Recalled by Cardiac Assist, Inc...

The Issue: Critical Failure of the LifeSPARC controller when the software freezes or...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 21, 2022· Medline Industries Inc.

Recalled Item: Medline CHEST TUBE REORDER NO: DYNJ36762A Recalled by Medline Industries...

The Issue: Due to a non-sterile component (tape) being place within the sterile portion...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2022· Getinge Usa Sales Inc

Recalled Item: Servo-air Ventilator System-The Servo-air Ventilator System is: Intended for...

The Issue: Device does not meet regulatory requirements of stability while stationary,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2022· Alcor Scientific, Inc.

Recalled Item: iSED Primary Pump Tubing Spare Part Kit- (IVD) tubing is Recalled by Alcor...

The Issue: Primary Pump Tubing Spare Part is incorrect. If the tubing is installed onto...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2022· Qiagen Sciences LLC

Recalled Item: FGFR RGQ RT-PCR Kit (RUO Recalled by Qiagen Sciences LLC Due to Increased...

The Issue: Increased occurrence rate of false positive results, lead to a false...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2022· Qiagen Sciences LLC

Recalled Item: therascreen FGFR RGQ RT-PCR Kit (CE IVD Recalled by Qiagen Sciences LLC Due...

The Issue: Increased occurrence rate of false positive results, lead to a false...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2022· Qiagen Sciences LLC

Recalled Item: therascreen FGFR RGQ RT-PCR kit (US IVD) Recalled by Qiagen Sciences LLC Due...

The Issue: Increased occurrence rate of false positive results, lead to a false...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2022· Aizu Olympus Co., Ltd.

Recalled Item: EVIS EXERA III Bronchovideoscope Recalled by Aizu Olympus Co., Ltd. Due to...

The Issue: The recalled unit was utilized in a veterinary endoscopy procedure in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2022· Getinge Usa Sales Inc

Recalled Item: Maquet Critical Care AB/Getinge Servo-u Ventilator System Recalled by...

The Issue: Ventilators may generate a combination of alarms which may result in loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 20, 2022· bioMerieux, Inc.

Recalled Item: NUCLISENS easyMAG Magnetic Silica Recalled by bioMerieux, Inc. Due to There...

The Issue: There is a potential of no result leading to possible delayed result due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· NuVasive Inc

Recalled Item: NuVasive MD Pulse III Multimodality System Pulse Software Recalled by...

The Issue: Due to an incorrect security key, customers were unable to connect to remote...

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

Class III — Low RiskOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner PC Hydrophilic Wire Guide PART NUMBER (RPN): RFSPC-35-180...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWAS-35-150...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner PC Hydrophilic Wire Guide PART NUMBER (RPN):RLPC-35-180 ORDER...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner PC Hydrophilic Wire Guide PART NUMBER (RPN): RPC-35-180 Recalled...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWS-35-80...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWS-35-150...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWA-18-150...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner PC Hydrophilic Wire Guide PART NUMBER (RPN)RFPC-35-180 ORDER...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPW-35-150...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing