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 40414060 of 13,606 recalls

DrugApril 19, 2021· SigmaPharm Laboratories LLC

Recalled Item: Asenapine Sublingual Tablets Recalled by SigmaPharm Laboratories LLC Due to...

The Issue: Incorrect Product Formulation; product was manufactured with the incorrect...

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

Class III — Low RiskOngoing
Refund
DrugApril 16, 2021· Noven Pharmaceuticals Inc

Recalled Item: Estradiol Transdermal System Delivers 0.0375 mg/day Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for release rate testing and...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 16, 2021· Noven Pharmaceuticals Inc

Recalled Item: Minivelle (estradiol transdermal system) Delivers 0.075 mg/day Recalled by...

The Issue: Defective Delivery System: Out of specification for release rate testing and...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 15, 2021· Grace Healthcare Medical, Inc

Recalled Item: Oxygen Recalled by Grace Healthcare Medical, Inc 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
DrugApril 14, 2021· Fresenius Medical Care, North America

Recalled Item: Delflex Peritoneal Dialysis Solution with 1.5% Dextrose Recalled by...

The Issue: Labeling; Label Mix-up; 4.25% DEXTROSE bag was found inside a 1.5% DEXTROSE box.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2021· Nomax Inc

Recalled Item: Dry Eye Test Recalled by Nomax Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugApril 12, 2021· Edge Pharma, LLC

Recalled Item: Betadine (Povidone-Iodine) 5% Recalled by Edge Pharma, LLC Due to Defective...

The Issue: Defective container; syringe content migrating past the seal of the plunger...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 9, 2021· Teligent Pharma, Inc.

Recalled Item: Flurandrenolide Ointment USP Recalled by Teligent Pharma, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications:

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 8, 2021· NSNY Distributor Inc

Recalled Item: Ginseng Power 5000 capsule Recalled by NSNY Distributor Inc Due to...

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 8, 2021· NSNY Distributor Inc

Recalled Item: Premium OrgaZEN 7000 capsule Recalled by NSNY Distributor Inc Due to...

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 6, 2021· Hyobin LLC

Recalled Item: PremierZen Black 5000 Recalled by Hyobin LLC Due to Marketed without...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2021· Hyobin LLC

Recalled Item: Triple SupremeZen Plus 3500 Recalled by Hyobin LLC Due to Marketed without...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2021· Hyobin LLC

Recalled Item: PremierZen Extreme 3000 Recalled by Hyobin LLC Due to Marketed without...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 1, 2021· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Itraconazole Capsules Recalled by Jubilant Cadista Pharmaceuticals, Inc. Due...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2021· QMart

Recalled Item: IMPERIAL GOLD 2000 Recalled by QMart Due to Marketed without Approved...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2021· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Riomet (metformin hydrochloride oral solution) 500 mg/5 mL Cherry Flavor...

The Issue: Microbial Contamination of Non-Sterile Product

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2021· QMart

Recalled Item: Burro en Primavera Recalled by QMart Due to Marketed without Approved...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2021· QMart

Recalled Item: Imperial Platinum 2000 Recalled by QMart Due to Marketed without Approved...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2021· QMart

Recalled Item: PremierZen Extreme 3000 Recalled by QMart Due to Marketed without Approved...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2021· Apotex Corp.

Recalled Item: Guanfacine Extended-Release Tablets 2 mg Recalled by Apotex Corp. Due to...

The Issue: Cross Contamination with Other Product: Product is being recalled due to...

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

Class II — Potential Health HazardOngoing
Refund