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 41214140 of 13,606 recalls

DrugMarch 4, 2021· Teva Pharmaceuticals USA

Recalled Item: Romidepsin Injecton Recalled by Teva Pharmaceuticals USA Due to Failed...

The Issue: Failed Impurity/Degradation Specifications: Out-of-specifications results...

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

Class III — Low RiskOngoing
Refund
DrugMarch 2, 2021· Ferring Pharmaceuticals Inc

Recalled Item: Menopur 75 IU Recalled by Ferring Pharmaceuticals Inc Due to Failed pH...

The Issue: Failed pH specifications: Out of Specification pH results for 0.9% Sodium...

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

Class III — Low RiskOngoing
Refund
DrugMarch 2, 2021· A-S Medication Solutions LLC.

Recalled Item: Acetaminophen Recalled by A-S Medication Solutions LLC. Due to Labeling:...

The Issue: Labeling: Label Mix-up; The bottle of over-the-counter Acetaminophen 500mg...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 26, 2021· Alvogen, Inc

Recalled Item: Buprenorphine and Naloxone Sublingual Film 2mg/0.5mg Recalled by Alvogen,...

The Issue: Subpotent drug: Out of specification for assay of naloxone and buprenorphine...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 26, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Progesterone Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed Dissolution Specifications: Out-of-specification results observed for...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2021· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Cequa (cyclosporine ophthalmic solution) 0.09% Recalled by SUN...

The Issue: Subpotent

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

Class III — Low RiskOngoing
Refund
DrugFebruary 19, 2021· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 20 mg over 9 hours...

The Issue: Defective Delivery System: Out of specification for mechanical peel.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 19, 2021· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for mechanical peel.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 19, 2021· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Methylprednisolone Tablets USP Recalled by Jubilant Cadista Pharmaceuticals,...

The Issue: Labeling: Illegible label: Customer complaint received of mis-alignment...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 19, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...

The Issue: Failed Impurities/Degradation Specifications:presence of ATV cyclo IP and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 19, 2021· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 30 mg over 9 hours...

The Issue: Defective Delivery System: Out of specification for mechanical peel.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 19, 2021· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for mechanical peel.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 18, 2021· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Acyclovir Sodium Injection 1000mg/20mL (50mg/mL) vial NDC 68382-049-01...

The Issue: Crystallization: customer complaints for crystallization in finished product.

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 18, 2021· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Acyclovir Sodium Injection 500mg/10mL (50mg/mL) vial NDC 68382-048-01...

The Issue: Crystallization: customer complaints for crystallization in finished product.

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 17, 2021· Edge Pharma, LLC

Recalled Item: Methacholine Challenge 5-Syringe Test Kits Recalled by Edge Pharma, LLC Due...

The Issue: Temperature Abuse; labeled with the incorrect room temperature (15-25 ¿C)...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 17, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Imatinib Mesylate Tablets 100mg Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2021· Teva Pharmaceuticals USA

Recalled Item: Metoclopramide Injection USP Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Chemical contamination; Unknown brown residue adhering to the inside of one...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2021· Adams.Secret.co

Recalled Item: Adam's Secret Extra Strength 1500 Recalled by Adams.Secret.co Due to...

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 I — Serious Health HazardOngoing
Refund
DrugFebruary 15, 2021· Adams.Secret.co

Recalled Item: Adam's Secret Extra Strength 3000 Recalled by Adams.Secret.co Due to...

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 I — Serious Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Sterile Diluent for Epoprostenol Sodium for Injection Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund