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 1296112980 of 13,463 recalls

DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: libigrow capsules Recalled by Performance Plus Marketing, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: Mojo nights SUPREME Capsules Recalled by Performance Plus Marketing, Inc....

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· Pacira Pharmaceuticals, Inc.

Recalled Item: EXPAREL (bupivacaine liposome injectable suspension) Recalled by Pacira...

The Issue: Subpotent; bupivacaine

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2012· L. Perrigo Co.

Recalled Item: Prednisone tablets Recalled by L. Perrigo Co. Due to Presence of Foreign...

The Issue: Presence of Foreign Substance(s); Perrigo has been notified of a recall by...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: CASANOVA Capsules Recalled by Performance Plus Marketing, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: Mojo nights Capsules Recalled by Performance Plus Marketing, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 14, 2012· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets Recalled by Mylan...

The Issue: Superpotent (Multiple Ingredient) Drug: Oversized tablets resulting in...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 13, 2012· Watson Laboratories Inc

Recalled Item: Caziant (desogestrel and ethinyl estradiol) Tablets Recalled by Watson...

The Issue: Impurities/Degradation Products: Out-of-specification results were obtained...

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

Class III — Low RiskOngoing
Refund
DrugDecember 12, 2012· Schering-Plough Products, LLC

Recalled Item: Temodar (temozolomide) Capsule Recalled by Schering-Plough Products, LLC Due...

The Issue: Failed Impurities/Degradation Specifications: The recall is being initiated...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 12, 2012· Boehringer Ingelheim Roxane Inc

Recalled Item: Perindopril Erbumine Tablets Recalled by Boehringer Ingelheim Roxane Inc Due...

The Issue: Impurities/Degradation Products: Out of Specification results found for...

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

Class III — Low RiskOngoing
Refund
DrugDecember 10, 2012· Upsher Smith Laboratories, Inc.

Recalled Item: Divalproex Sodium Delayed-Release Tablets Recalled by Upsher Smith...

The Issue: Labeling: Label Error On Declared Strength; Some bottles of product were...

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

Class III — Low RiskOngoing
Refund
DrugDecember 10, 2012· Brower Enterprises Inc

Recalled Item: WOW Recalled by Brower Enterprises Inc Due to Undeclared Drug

The Issue: Marketed without an Approved NDA/ANDA: Brower Enterprises Inc., is recalling...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 7, 2012· West-ward Pharmaceutical Corp.

Recalled Item: Lisinopril Tablets Recalled by West-ward Pharmaceutical Corp. Due to...

The Issue: Presence of Foreign Substance: Uncharacteristic black spots identified as a...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2012· West-ward Pharmaceutical Corp.

Recalled Item: Propylthiouracil Tablets Recalled by West-ward Pharmaceutical Corp. Due to...

The Issue: Presence of Foreign Substance: Uncharacteristic spots identified as steel...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2012· Bayer Healthcare, LLC

Recalled Item: Bronkaid Dual Action Formula Recalled by Bayer Healthcare, LLC Due to...

The Issue: Labeling: Label lacks warning or Rx legend; Certain information was...

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

Class III — Low RiskOngoing
Refund
DrugDecember 7, 2012· West-ward Pharmaceutical Corp.

Recalled Item: Carisoprodol Tablets Recalled by West-ward Pharmaceutical Corp. Due to...

The Issue: Presence of Foreign Substance: Uncharacteristic blacks spots on tablets.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2012· Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Recalled Item: Hydrocodone bitartrate and acetaminophen Tablets Recalled by Vintage...

The Issue: Superpotent (Multiple Ingredient) Drug: Complaint received of oversized tablets.

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 5, 2012· Teva Pharmaceuticals USA, Inc.

Recalled Item: Copaxone (glatiramer acetate injection) Recalled by Teva Pharmaceuticals...

The Issue: Presence of Foreign Substance: Product is being recalled due to receiving an...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 5, 2012· West-ward Pharmaceutical Corp.

Recalled Item: PredniSONE Tablets Recalled by West-ward Pharmaceutical Corp. Due to...

The Issue: Presence of Foreign Substance: Tablets are being recalled due to gray...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 5, 2012· West-ward Pharmaceutical Corp.

Recalled Item: PredniSONE Tablets Recalled by West-ward Pharmaceutical Corp. Due to...

The Issue: Presence of Foreign Substance: A complaint was received for black specks...

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

Class II — Potential Health HazardOngoing
Refund