Product Recalls in Tennessee

Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,645 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,645 in last 12 months

Showing 1260112620 of 13,463 recalls

DrugMay 20, 2013· Dolphin Intertrade Corporation

Recalled Item: JaDera Recalled by Dolphin Intertrade Corporation Due to Undeclared Sibutramine

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
DrugMay 20, 2013· Dolphin Intertrade Corporation

Recalled Item: XIYOUJI QINGZHI CAPSULE Recalled by Dolphin Intertrade Corporation 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
DrugMay 17, 2013· Warner Chilcott US LLC

Recalled Item: Enablex (darifenacin) Extended Release Tablet Recalled by Warner Chilcott US...

The Issue: Failed Impurities/Degradation Specifications: unspecified degradation product

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 16, 2013· West-Ward Pharmaceutical Corp.

Recalled Item: West-ward Belladonna Alkaloids with Phenobarbital Tablets Recalled by...

The Issue: Cross contamination with other products: Belladonna Alkaloids with...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 16, 2013· Hospira Inc.

Recalled Item: Diazepam Injection Recalled by Hospira Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 16, 2013· West-Ward Pharmaceutical Corp.

Recalled Item: West-ward Belladonna Alkaloids with Phenobarbital Tablets Recalled by...

The Issue: Presence of Foreign Substance: Belladonna Alkaloids with Phenobarbital...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 15, 2013· Actavis South Atlantic LLC

Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution USP) 15 mg/mL Recalled by Actavis...

The Issue: Failed Impurity/Degradation Specification; "Related Compound C"

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 15, 2013· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Budesonide Capsules Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Failed Dissolution Specifications: Routine stability testing at the 12-month...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Theraflu Nighttime Warming Relief Nighttime Multi-Symptom Cold Recalled by...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Excedrin Recalled by Novartis Consumer Health Due to Failed...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Maximum Strength Comtrex Recalled by Novartis Consumer Health Due to Failed...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Maximum Strength Comtrex Recalled by Novartis Consumer Health Due to Failed...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Theraflu Warming Relief Recalled by Novartis Consumer Health Due to Failed...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Maximum Strength Comtrex Day/Night Cold & Cough Recalled by Novartis...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Maximum Strength Comtrex Nighttime Cold & Cough Recalled by Novartis...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 13, 2013· Abrams Royal Pharmacy

Recalled Item: Trace Mineral-5 MDV Recalled by Abrams Royal Pharmacy Due to Non-Sterility;...

The Issue: Non-Sterility; contract laboratory identified Staphylococcus warneri in the...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 13, 2013· West-ward Pharmaceutical Corp.

Recalled Item: Nicardipine Hydrochloride Injection 25 mg/10 mL (2.5 mg/mL) Recalled by...

The Issue: Failed Impurity/Degradation Specifications; out of specification value for...

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

Class III — Low RiskOngoing
Refund
DrugMay 13, 2013· Zydus Pharmaceuticals USA Inc

Recalled Item: Warfarin Sodium Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: Failed Tablet/Capsule Specifications: A product complaint was received from...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 10, 2013· Apotex Corp.

Recalled Item: Piperacillin and Tazobactam for Injection Recalled by Apotex Corp. Due to...

The Issue: Crystallization: Potential to exhibit precipitation/crystallization in IV...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 7, 2013· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS (fluocinolone acetonide) Topical Oil (SCALP OIL) Recalled...

The Issue: Subpotent Drug: the active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund