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. 1,042 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,042 in last 12 months

Showing 18381–18400 of 54,363 recalls

Medical DeviceNovember 11, 2020· Westmed, Inc.

Recalled Item: Recalled by Westmed, Inc. Due to There is a potential that the fitment...

The Issue: There is a potential that the fitment between the oxygen delivery tube and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2020· Westmed, Inc.

Recalled Item: Recalled by Westmed, Inc. Due to There is a potential that the fitment...

The Issue: There is a potential that the fitment between the oxygen delivery tube and...

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

Class II — Potential Health HazardOngoing
DrugNovember 11, 2020· Teva Pharmaceuticals USA

Recalled Item: Testosterone Gel 1% Recalled by Teva Pharmaceuticals USA Due to Superpotent...

The Issue: Superpotent Drug: High out-of-specification assay results were obtained...

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

Class III — Low RiskOngoing
Refund
DrugNovember 11, 2020· Apotex Corp.

Recalled Item: Aripiprazole Tablets Recalled by Apotex Corp. Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications: Out of specification for dissolution.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2020· InvaTech Pharma Solutions, LLC

Recalled Item: Levocetirizine Dihydrochloride Tablets Recalled by InvaTech Pharma...

The Issue: Failed Impurities/Degradation Specifications: One lot of Levocetirizine...

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

Class III — Low RiskOngoing
Refund
DrugNovember 10, 2020· EYWA PHARMA INC

Recalled Item: Levetiracetam Tablets Recalled by EYWA PHARMA INC Due to Presence of foreign...

The Issue: Presence of foreign tablet/capsule: A 1000 mg Levetiracetam Tablet was found...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 10, 2020· Applied Medical Technology Inc

Recalled Item: AMT Male ENFit-to-Stepped Male (Christmas Tree) Adapter Recalled by Applied...

The Issue: The products subject to this recall may contain obvious, incorrect pouch...

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

Class III — Low RiskOngoing
Medical DeviceNovember 10, 2020· CryoLife, Inc.

Recalled Item: CryoValve SG Pulmonary Human Heart Valve. The valve is cryopreserved...

The Issue: On November 10, 2020, it was discovered that there are post- processing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2020· CryoLife, Inc.

Recalled Item: CryoPatch SG Pulmonary Human Cardiac Patch. The patch is cryopreserved...

The Issue: On November 10, 2020, it was discovered that there are post- processing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2020· TissueTech, Inc.

Recalled Item: PROKERA Slim Recalled by TissueTech, Inc. Due to Potential exposure of...

The Issue: Potential exposure of product to microbial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2020· TissueTech, Inc.

Recalled Item: PROKERA Plus Recalled by TissueTech, Inc. Due to Potential exposure of...

The Issue: Potential exposure of product to microbial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2020· TissueTech, Inc.

Recalled Item: PROKERA Recalled by TissueTech, Inc. Due to Potential exposure of product to...

The Issue: Potential exposure of product to microbial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2020· Baxter Healthcare Corporation

Recalled Item: MiniCap Extended Life PD Transfer Set Recalled by Baxter Healthcare...

The Issue: Potential for no-flow and leaks under the twist clamp.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2020· ROi CPS LLC

Recalled Item: Custom procedure packs Recalled by ROi CPS LLC Due to Gauze sponges...

The Issue: Gauze sponges contained in custom kits may be flaking or fraying.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2020· Shimadzu Medical Systems

Recalled Item: Shimadzu Mobile X-Ray System Recalled by Shimadzu Medical Systems Due to...

The Issue: There is a potential that the adjustable handle option on the X-Ray system...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2020· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Prime SP Recalled by Canon Medical System, USA, INC. Due to A...

The Issue: A software problem has been identified which could result in the CT Scanner...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2020· ICU Medical, Inc.

Recalled Item: icumedical Cogent" Hemodynamic Monitoring System - Product Usage: intended...

The Issue: Due to a potential software issue, the display may show the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2020· Helena Laboratories, Corp.

Recalled Item: K-ACT Actalyke Clotting Test Tubes that are used in the: Recalled by Helena...

The Issue: Due to complaints received associated with cracked/split test tube caps.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Citrasate Liquid Acid concentrate drums Recalled by Fresenius Medical Care...

The Issue: The sodium and/or calcium levels in these concentrates were below the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: NaturaLyte Liquid Acid concentrate bottles Recalled by Fresenius Medical...

The Issue: The sodium and/or calcium levels in these concentrates were below the...

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

Class II — Potential Health HazardOngoing