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. 2,812 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
2,812 in last 12 months

Showing 40214040 of 54,363 recalls

Medical DeviceNovember 12, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Magnesium Flex reagent cartridge Recalled by Siemens Healthcare Diagnostics,...

The Issue: Siemens Healthcare Diagnostics is recalling two lots of their Dimension...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: ST OR MAYO HEGAR NEEDLEHOLDER 6"(OR2500) Recalled by MEDLINE INDUSTRIES, LP...

The Issue: Weak seals may result in a breach of sterility, which may not be detectable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: STERILE MAGILL FORCEP (MAGF9) Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Weak seals may result in a breach of sterility, which may not be detectable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: O.R. SCISSORS Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Weak...

The Issue: Weak seals may result in a breach of sterility, which may not be detectable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: RUMMELL Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Weak seals...

The Issue: Weak seals may result in a breach of sterility, which may not be detectable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: STERILE STRT KELLY HEMOSTAT (SK8039S) Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Weak seals may result in a breach of sterility, which may not be detectable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: ST IUD REMOVAL HOOK 10" (504090) Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Weak seals may result in a breach of sterility, which may not be detectable...

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

Class II — Potential Health HazardOngoing
DrugNovember 11, 2024· American Regent, Inc.

Recalled Item: Venofer (iron sucrose) Injection Recalled by American Regent, Inc. Due to...

The Issue: Presence of Particulate Matter: Potential for glass delamination from the vials.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2024· American Regent, Inc.

Recalled Item: Venofer (iron sucrose) Injection Recalled by American Regent, Inc. Due to...

The Issue: Presence of Particulate Matter: Potential for glass delamination from the vials.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2024· American Regent, Inc.

Recalled Item: Venofer (iron sucrose) Injection Recalled by American Regent, Inc. Due to...

The Issue: Presence of Particulate Matter: Potential for glass delamination from the vials.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2024· Safecor Health, LLC

Recalled Item: Aspirin Chewable tablet 81 mg Recalled by Safecor Health, LLC Due to cGMP...

The Issue: cGMP Deviations: Observations were made that some blister card-foils were...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2024· Safecor Health, LLC

Recalled Item: Calcium Carbonate Chewable 500 mg Recalled by Safecor Health, LLC Due to...

The Issue: cGMP Deviations: Observations were made that some blister card-foils were...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2024· Safecor Health, LLC

Recalled Item: Docusate Sodium 250 mg Recalled by Safecor Health, LLC Due to cGMP...

The Issue: cGMP Deviations: Observations were made that some blister card-foils were...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2024· Safecor Health, LLC

Recalled Item: Vitamin B1 Recalled by Safecor Health, LLC Due to cGMP Deviations:...

The Issue: cGMP Deviations: Observations were made that some blister card-foils were...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2024· Safecor Health, LLC

Recalled Item: Vitamin D3 Recalled by Safecor Health, LLC Due to cGMP Deviations:...

The Issue: cGMP Deviations: Observations were made that some blister card-foils were...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 11, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Allura Xper Systems (R7.6-R8.1). Labeled as the following: 1....

The Issue: Potential safety issues in Allura Xper R7.6- R8.1 systems where the Lifetime...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2024· Gauthier Biomedical, Inc.

Recalled Item: TriALTIS TORQUE LIMITER Recalled by Gauthier Biomedical, Inc. Due to An out...

The Issue: An out of specification component may result in the device exhibiting torque...

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

Class II — Potential Health HazardOngoing
FoodNovember 8, 2024· Wegmans Food Markets, Inc.

Recalled Item: Wegmans Large Asian Sesame Salad with Chicken and Asian Peanut Dressing....

The Issue: Contains undeclared egg

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 8, 2024· ACCORD HEALTHCARE, INC.

Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...

The Issue: Subpotent drug

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 8, 2024· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Presource Kits: 1) KIT Recalled by Cardinal Health 200, LLC...

The Issue: Potential for endotoxin contamination in non-sterile surgical strips and...

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

Class II — Potential Health HazardOngoing