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. 2,625 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,625 in last 12 months

Showing 1164111660 of 13,398 recalls

DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: Magic Slim capsules Recalled by MyNicNaxs, Inc. Due to Undeclared Active

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: REDUCE WEIGHT FRUTA PLANTA Capsules Recalled by MyNicNaxs, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: Super Fat Burning Bomb Capsules Recalled by MyNicNaxs, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: JIANFEIJINDAN Activity Girl Capsules Recalled by MyNicNaxs, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: SlimEasy Herbs Capsule Recalled by MyNicNaxs, Inc. Due to Undeclared Active

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: Pill for weight reduction Recalled by MyNicNaxs, Inc. Due to Undeclared Active

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· Teva Pharmaceuticals USA

Recalled Item: Teva Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Due...

The Issue: CGMP Deviations: Dextroamphetamine Saccharate, Amphetamine Asparate,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: Meizi Evolution Soft Gel Capsules Recalled by MyNicNaxs, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: Meizitang Strong Version Botanical Slimming Recalled by MyNicNaxs, Inc. Due...

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: Fruta BIO 400 mg capsules Recalled by MyNicNaxs, Inc. Due to Undeclared Active

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 22, 2014· Fresenius Kabi USA, LLC

Recalled Item: Heparin Sodium Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Subpotent; 18 month time point

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2014· The Mentholatum Co.

Recalled Item: ROHTO Redness Relief Recalled by The Mentholatum Co. Due to Lack of...

The Issue: Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2014· The Mentholatum Co.

Recalled Item: ROHTO Cooling Eye Drops Recalled by The Mentholatum Co. Due to Lack of...

The Issue: Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2014· The Mentholatum Co.

Recalled Item: ROHTO Redness Relief Recalled by The Mentholatum Co. Due to Lack of...

The Issue: Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2014· The Mentholatum Co.

Recalled Item: ROHTO Dry Eye Recalled by The Mentholatum Co. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2014· The Mentholatum Co.

Recalled Item: ROHTO Redness Relief Recalled by The Mentholatum Co. Due to Lack of...

The Issue: Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2014· Ranbaxy Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Ranbaxy Inc. Due to Presence of...

The Issue: Presence of Foreign Tablets: A product complaint was received by a...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 14, 2014· Mylan Pharmaceuticals Inc.

Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Subpotent Drug: Assay results obtained during stability testing for...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 14, 2014· Traxx International Corp

Recalled Item: Guaifenesin USP Recalled by Traxx International Corp Due to Presence of...

The Issue: Presence of Foreign Matter: Guaifenesin API powder is being recalled due to...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 13, 2014· Merck & Co Inc

Recalled Item: Liptruzet (ezetimibe and atorvastin) tablets Recalled by Merck & Co Inc Due...

The Issue: Defective Container; some of the outer laminate foil pouches allowed in air...

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

Class III — Low RiskOngoing
Refund