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. 2,801 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
2,801 in last 12 months

Showing 56815700 of 29,737 recalls

Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Pediatric Heart SJH Recalled by American Contract Systems, Inc. Due to...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Cath Cardiac Pack Recalled by American Contract Systems, Inc. Due to During...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Sub Q Recorder Pack Recalled by American Contract Systems, Inc. Due to...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Robotics Pack Recalled by American Contract Systems, Inc. Due to During an...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Breast Plastics Pack Recalled by American Contract Systems, Inc. Due to...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Pediatric Urology Wolson Pack Recalled by American Contract Systems, Inc....

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: General Pack Recalled by American Contract Systems, Inc. Due to During an...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· Siemens Medical Solutions USA, Inc

Recalled Item: (1) Over-ear headphones used with the MAGNETOM Amira MAGNETOM Free.Star...

The Issue: In some cases, when lubricating grease is present within the headband of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Pulmonx, Corp.

Recalled Item: Zephyr Endobronchial Valve (EBV) 5.5-LP Recalled by Pulmonx, Corp. Due to...

The Issue: Endobronchial implant devices may have been labeled with a shortened...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Access Vascular, Inc

Recalled Item: HydroPICC 5Fr Dual Lumen Recalled by Access Vascular, Inc Due to Specific...

The Issue: Specific lots of the Dual Lumen HydroPICC Kits were provided with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Access Vascular, Inc

Recalled Item: HydroPICC 5Fr Dual Lumen Maximal Barrier Kit Recalled by Access Vascular,...

The Issue: Specific lots of the Dual Lumen HydroPICC Kits were provided with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Philips North America Llc

Recalled Item: EarlyVue VS30 Vitals Monitor Recalled by Philips North America Llc Due to A...

The Issue: A software issue prevents the monitor from alarming when the high/low...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Philips North America Llc

Recalled Item: EarlyVue VS30 Vital Signs Monitor Recalled by Philips North America Llc Due...

The Issue: A software issue prevents the monitor from alarming when the high/low...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Smith & Nephew Inc

Recalled Item: smith&nephew LEGION OXINUM POSTERIOR STABILIZED NONPOROUS FERMOAL COMPONENT...

The Issue: The firm conducting a recall due to a complaint received indicating that a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCurity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCurity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing