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 1166111680 of 13,398 recalls

DrugJanuary 13, 2014· Merck & Co Inc

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

The Issue: This recall of LIPTRUZET is being initiated due to packaging defects. Some...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 13, 2014· Merck & Co Inc

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

The Issue: This recall of LIPTRUZET is being initiated due to packaging defects. Some...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 13, 2014· Merck & Co Inc

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

The Issue: This recall of LIPTRUZET is being initiated due to packaging defects. Some...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 13, 2014· HUMAN SCIENCE FOUNDATION

Recalled Item: PRO ArthMax Dietary Supplement tablets Recalled by HUMAN SCIENCE FOUNDATION...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the product to...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Calm & Correct Cream in 2 oz. containers with SKU number DM1020....

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Post Procedure Cream 1 oz. containers in the Dermamedics...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2014· Hospira Inc.

Recalled Item: DOBUTamine Injection Recalled by Hospira Inc. Due to Presence of Particulate...

The Issue: Presence of Particulate Matter: Discolored solution due to a chip in the...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Calm and Correct Serum Recalled by Dermamedics, L.L.C. Due to...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Post Procedure Cream Recalled by Dermamedics, L.L.C. Due to...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Complexion Repair Topical Rehydrating Emulsion which was...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Calm and Correct Cream 2 oz. containers in the Recalled by...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Baby's Relief Calm and Repair Cream in 2 oz. Recalled by...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2014· Dermamedics, L.L.C.

Recalled Item: Therametics Complexion Repair Topical Rehydrating Emulsion in 50 ml and...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Complexion Repair Topical Rehydrating Emulsion in 50 ml and...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 9, 2014· Hospira Inc.

Recalled Item: Aminosyn 3.5% M Sulfite-Free Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility; potential leakage from administrative port.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 9, 2014· Hospira Inc.

Recalled Item: Heparin Sodium 2000 USP Heparin Units per 1000 mL (2 Recalled by Hospira...

The Issue: Lack of Assurance of Sterility; potential leakage from administrative port.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 3, 2014· Dr. Reddy's Laboratories, Inc.

Recalled Item: a) Walgreens Lansoprazole Delayed Release Capsules Recalled by Dr. Reddy's...

The Issue: Microbial Contamination of Non-Sterile Products: Out-of-specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 2, 2014· Pfizer Inc.

Recalled Item: Zithromax (azithromycin for injection) Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Pfizer is recalling certain...

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

Class III — Low RiskOngoing
Refund
DrugDecember 27, 2013· Mangiacotti

Recalled Item: Mangiacotti - Lemon Verbena Hand Sanitizer Spray Recalled by Mangiacotti Due...

The Issue: Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 27, 2013· Mangiacotti

Recalled Item: Mangiacotti - Pomegranate Hand Sanitizer Spray Recalled by Mangiacotti Due...

The Issue: Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria...

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

Class II — Potential Health HazardOngoing
Refund