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. 2,006 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
2,006 in last 12 months

Showing 70617080 of 54,363 recalls

Medical DeviceJanuary 22, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS 3600 Immunodiagnostic System (New and ) Recalled by Ortho-Clinical...

The Issue: Potential For Aspiration from Unintended Sample Container During Sampling...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2024· Medtronic Neurosurgery

Recalled Item: Medtronic Duet External Drainage and Monitoring System Recalled by Medtronic...

The Issue: Potential for catheter disconnection from the patient line stopcock connectors.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : 31156 / COMBO KIT CONTAINS INS-8301 Recalled by Integra LifeSciences Corp....

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : INSHITHRZN / Integra Cranial Access Kit. For access Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : INS7260 / Integra¿ Cranial Access Kit. For access Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : INS7250 / Integra Cranial Access Kit. For access Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: INS7280 / Integra¿ Cranial Access Kit. For access to the Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : HITHSP04 / Integra Cranial Access Kit. For access Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : INS7270 / Integra¿ Cranial Access Kit. For access Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : INSHITH / Integra¿ Cranial Access Kit. For access Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : INSHITHND / Integra¿ Cranial access kit (without Prep Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· W.L. Gore & Associates, Inc.

Recalled Item: GORE VIABIL Short Wire Biliary Endoprosthesis Recalled by W.L. Gore &...

The Issue: Devices without transmural drainage holes may be mislabeled as devices with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : HITHSP06 / Integra Cranial Access Kit. For access Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : INS5HND / Integra Cranial access kit (without Prep Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
DrugJanuary 19, 2024· Bestco LLC

Recalled Item: CVS Health Cherry Cough Drops Recalled by Bestco LLC Due to CGMP Deviations:...

The Issue: CGMP Deviations: Potential Glass and Silicone particulates in product

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 19, 2024· OMEZA LLC

Recalled Item: Omeza Lidocaine Lavage pain relief oil 10*2mL VIALS Recalled by OMEZA LLC...

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 19, 2024· Bestco LLC

Recalled Item: Kroger Cherry Cough Drops Recalled by Bestco LLC Due to CGMP Deviations:...

The Issue: CGMP Deviations: Potential Glass and Silicone particulates in product

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 19, 2024· Bestco LLC

Recalled Item: Equate Cherry Cough Drops Recalled by Bestco LLC Due to CGMP Deviations:...

The Issue: CGMP Deviations: Potential Glass and Silicone particulates in product

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 19, 2024· Bestco LLC

Recalled Item: Family Wellness Cherry Cough Drops Menthol cough suppressant/Oral Anesthetic...

The Issue: CGMP Deviations: Potential Glass and Silicone particulates in product

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 19, 2024· OMEZA LLC

Recalled Item: Omeza Skin Protectant Recalled by OMEZA LLC Due to CGMP Deviations

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund