Product Recalls in Kentucky

Product recalls affecting Kentucky — including food, drugs, consumer products, medical devices, and vehicles distributed to Kentucky. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,609 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,609 in last 12 months

Showing 1290112920 of 13,398 recalls

DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: BLUE Diamond PLATINUM 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 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: 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 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: 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 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· 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· 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: 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
DrugDecember 4, 2012· Green Valley Drugs

Recalled Item: Methylprednisolone Preservative Free 40 mg/ml Injectible Suspension Recalled...

The Issue: Non-Sterility: Green Valley Drugs received positive sterility results from...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 4, 2012· Green Valley Drugs

Recalled Item: Cyanocobalamin 1000 mcg/ml Recalled by Green Valley Drugs Due to...

The Issue: Non-Sterility: Green Valley Drugs received positive sterility results from...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 4, 2012· Amedra Pharmaceuticals LLC

Recalled Item: Dextroamphetamine Sulfate Extended Release Capsules Recalled by Amedra...

The Issue: Failed Dissolution Specifications: The affected lots may not meet the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2012· Amedra Pharmaceuticals LLC

Recalled Item: Dextroamphetamine Sulfate Extended Release Capsules Recalled by Amedra...

The Issue: Failed Dissolution Specifications: The affected lots may not meet the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2012· Amedra Pharmaceuticals LLC

Recalled Item: Dextroamphetamine Sulfate Extended Release Capsules Recalled by Amedra...

The Issue: Failed Dissolution Specifications: The affected lots may not meet the...

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

Class II — Potential Health HazardOngoing
Refund