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. 2,779 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
2,779 in last 12 months

Showing 1164111660 of 13,606 recalls

DrugApril 17, 2014· Wockhardt Usa Inc.

Recalled Item: Wockhardt Metoprolol Succinate Recalled by Wockhardt Usa Inc. Due to Failed...

The Issue: Failed Dissolution Specifications: Product was out of specification (OOS) at...

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

Class III — Low RiskOngoing
Refund
DrugApril 17, 2014· Cubist Pharmaceuticals, Inc.

Recalled Item: CUBICIN (daptomycin for injection) Recalled by Cubist Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter: Customer complaint stating that one vial...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 16, 2014· Pfizer Us Pharmaceutical Group

Recalled Item: Pristiq (desvenlafaxine) Extended-Release Tablets 50 mg Recalled by Pfizer...

The Issue: Presence of Foreign Tablets/Capsules: Pfizer is recalling 50 mg Pristiq...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 15, 2014· P&L Developments, LLC

Recalled Item: Children's Triacting Night Time Cold & Cough with PE (diphenhydramine...

The Issue: Presence of Precipitate: Small amounts of diphenydramine and mannitol...

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

Class III — Low RiskOngoing
Refund
DrugApril 15, 2014· Sung Soo Kim

Recalled Item: Super ARTHGOLD 500mg Recalled by Sung Soo Kim Due to Undeclared Indomethacin

The Issue: Marketed Without an Approved NDA/ANDA; Product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 14, 2014· Upsher Smith Laboratories, Inc.

Recalled Item: Oxandrolone Tablets Recalled by Upsher Smith Laboratories, Inc. Due to...

The Issue: Labeling: Missing Label; Three cases of product (total of 36 bottles) were...

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

Class III — Low RiskOngoing
Refund
DrugApril 14, 2014· P&L Developments, LLC

Recalled Item: Day Time Cold & Flu Recalled by P&L Developments, LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: Phenylephrine component is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugApril 14, 2014· Golden State Medical Supply Inc.

Recalled Item: LOSARTAN POTASSIUM Tablets Recalled by Golden State Medical Supply Inc. Due...

The Issue: Presence of Foreign Substance; some bottles may contain debris that was...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 14, 2014· Fresenius Kabi USA LLC

Recalled Item: HALOPERIDOL DECANOATE INJECTION Recalled by Fresenius Kabi USA LLC Due to...

The Issue: Failed Impurities/Degradation Specifications: Fresenius Kabi is recalling...

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

Class III — Low RiskOngoing
Refund
DrugApril 11, 2014· Aaron Industries Inc

Recalled Item: Maximum Strength/Non-Drowsy Tussin DM Adult Maximum Strength Recalled by...

The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...

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

Class III — Low RiskOngoing
Refund
DrugApril 10, 2014· Bausch & Lomb, Inc.

Recalled Item: Muro 128 (sodium chloride) hypertonicity ophthalmic ointment Recalled by...

The Issue: Crystallization: Crystal precipitate formation and an increase in the number...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 10, 2014· Bausch & Lomb, Inc.

Recalled Item: Sodium Chloride Hypertonicity Ophthalmic Ointment Recalled by Bausch & Lomb,...

The Issue: Crystallization: Crystal precipitate formation and an increase in the number...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 10, 2014· Wockhardt Usa Inc.

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Wockhardt Usa Inc....

The Issue: Failed Dissolution Specifications: Failure of dissolution test observed at...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 9, 2014· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: Cetirizine Hydrochloride Chewable Tablets Recalled by Caraco Pharmaceutical...

The Issue: Failed Impurities/Degradation Specifications: out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugApril 9, 2014· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: Children's Cetirizine Hydrochloride Chewable Tablets Recalled by Caraco...

The Issue: Failed Impurities/Degradation Specifications: out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugApril 9, 2014· Nature's Universe

Recalled Item: THINOGENICS Recalled by Nature's Universe Due to Undeclared Sibutramine

The Issue: Marketed Without an Approved NDA/ANDA: Product contains undeclared sibutramine.

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 8, 2014· Pfizer Inc.

Recalled Item: Tikosyn¿ (dofetilide) 500 mcg (0.5mg) capsules Recalled by Pfizer Inc. Due...

The Issue: Presence of Foriegn Tablets/Capsules: A single Tikosyn¿ (dofetilide) 250 mcg...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 7, 2014· Teva Pharmaceuticals USA

Recalled Item: BUPRENORPHINE HYDROCHLORIDE Sublingual Tablets Recalled by Teva...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 7, 2014· Piramal Critical Care, Inc.

Recalled Item: Sevoflurane Recalled by Piramal Critical Care, Inc. Due to Failed pH...

The Issue: Failed pH Specifications: product was too acidic.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 7, 2014· Teva Pharmaceuticals USA

Recalled Item: BUPRENORPHINE HYDROCHLORIDE Sublingual Tablets Recalled by Teva...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

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

Class II — Potential Health HazardOngoing
Refund