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 1202112040 of 13,398 recalls

DrugJuly 22, 2013· Mira Health Products Ltd.

Recalled Item: METHA-DROL Extreme capsules Recalled by Mira Health Products Ltd. Due to...

The Issue: Marketed without an Approved NDA/ANDA; product found to contain dimethazine...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 22, 2013· Mira Health Products Ltd.

Recalled Item: B-50 capsules Recalled by Mira Health Products Ltd. Due to Marketed without...

The Issue: Marketed without an Approved NDA/ANDA; product found to contain methasterone...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 22, 2013· Mira Health Products Ltd.

Recalled Item: Super-DMZ Rx 2.0 Capsules Recalled by Mira Health Products Ltd. Due to...

The Issue: Marketed without an Approved NDA/ANDA; product contains the steroid...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelder Fem Mezcla con L-Carnitina Suplemento Alimenticio Recalled by...

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
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelin Siloutte Te Recalled by Herbal Give Care Llc Due to Undeclared...

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
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelin Siloutte Mezcal Herbal con L-Carnitine Suplemento Alimenticio...

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
DrugJuly 19, 2013· Myson Corporation, Inc.

Recalled Item: Volcano Male Enhancement Liquid Recalled by Myson Corporation, Inc. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: All lots of Volcano Liquid and...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelder Siloutte Suplemento Alimenticio Recalled by Herbal Give Care Llc...

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
DrugJuly 19, 2013· Myson Corporation, Inc.

Recalled Item: Volcano Male Enhancement 1500mg Recalled by Myson Corporation, Inc. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: All lots of Volcano Liquid and...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelder Man Herbal Blend With L-Carnitine Dietary Supplement Recalled by...

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
DrugJuly 19, 2013· Watson Laboratories Inc

Recalled Item: Oxycodone and Acetaminophen Capsules Recalled by Watson Laboratories Inc Due...

The Issue: Subpotent drug: Two lots of Oxycodone and Acetaminophen Capsules, USP 5/500...

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

Class III — Low RiskOngoing
Refund
DrugJuly 19, 2013· Bracco Diagnostics Inc

Recalled Item: Tagitol V Barium Sulfate Suspension (40% w/v Recalled by Bracco Diagnostics...

The Issue: Failed Stability Specifications: Tagitol V Barium Sulfate Lot #65846 sampled...

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

Class III — Low RiskOngoing
Refund
DrugJuly 18, 2013· GlaxoSmithKline, LLC.

Recalled Item: TUMS Recalled by GlaxoSmithKline, LLC. Due to Presence of Foreign...

The Issue: Presence of Foreign Tablets/Capsules: Product labeled TUMS Ultra Assorted...

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

Class III — Low RiskOngoing
Refund
DrugJuly 18, 2013· Vi-Jon, Inc.

Recalled Item: ALCOHOL FREE ANTISEPTIC (cetylpyridinium chloride) Mouth Rinse Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products: This product is being...

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

Class III — Low RiskOngoing
Refund
DrugJuly 17, 2013· Apotex Inc.

Recalled Item: Acyclovir Tablets USP 800 mg Recalled by Apotex Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Product from lot KF2199, may contain tablets...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2013· Hospira Inc.

Recalled Item: 0.25% Bupivacaine HCl Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of particulate matter: visible free floating and partially embedded...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 12, 2013· Hospira Inc.

Recalled Item: 0.75% Bupivacaine HCl Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of particulate matter: visible free floating and partially embedded...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 4, 2013· VistaPharm, Inc.

Recalled Item: Nystatin Oral Suspension Recalled by VistaPharm, Inc. Due to Failed...

The Issue: Failed Impurites/Degradation Specifications: Test failure of single largest...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 3, 2013· Procter & Gamble Co

Recalled Item: DayQuil Sinex DayTime Sinus Relief (acetaminophen 325 mg and phenylephrine...

The Issue: Unit Dose Mispackaging: Product packaging defect which could result in code...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2013· Core Pharma Llc

Recalled Item: Pyridostigmine Bromide Tablets 60 mg Recalled by Core Pharma Llc Due to...

The Issue: Failed Stability Specifications: Pyridostigmine Bromide tablets, is being...

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

Class II — Potential Health HazardOngoing
Refund