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. 2,656 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,656 in last 12 months

Showing 43414360 of 13,398 recalls

DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: WP Thyroid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: Nature-Throid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: WP Thyroid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: WP Thyroid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: Nature Throid Recalled by RLC Labs Inc. Due to Subpotent Drug: FDA analysis...

The Issue: Subpotent Drug: FDA analysis found product to be subpotent

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: Nature-Throid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: WP Thyroid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: Nature Throid Recalled by RLC Labs Inc. Due to Subpotent Drug: FDA analysis...

The Issue: Subpotent Drug: FDA analysis found product to be subpotent

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: Nature Throid Recalled by RLC Labs Inc. Due to Subpotent Drug: FDA analysis...

The Issue: Subpotent Drug: FDA analysis found product to be subpotent

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 24, 2020· Strides Inc.

Recalled Item: Strides Pharma Inc.Potassium Chloride Extended-Release Tablets Recalled by...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2020· Teva Pharmaceuticals USA

Recalled Item: Cephalexin for Oral Suspension Recalled by Teva Pharmaceuticals USA Due to...

The Issue: CGMP deviations; there is a possibility that some bottles in these lots may...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2020· Teva Pharmaceuticals USA

Recalled Item: Cephalexin for Oral Suspension Recalled by Teva Pharmaceuticals USA Due to...

The Issue: CGMP deviations; there is a possibility that some bottles in these lots may...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2020· Teva Pharmaceuticals USA

Recalled Item: Cephalexin for Oral Suspension Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Sub-Potent Drug: Out of specification test results for potency (below...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 19, 2020· BAYSHORE PHARMACEUTICALS

Recalled Item: Metformin Hydrochloride Extended-Release Tablets USP Recalled by BAYSHORE...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 19, 2020· BAYSHORE PHARMACEUTICALS

Recalled Item: Metformin Hydrochloride Extended-Release Tablets USP Recalled by BAYSHORE...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2020· Mylan Institutional LLC

Recalled Item: Amiodarone Hydrochloride Injection Recalled by Mylan Institutional LLC Due...

The Issue: Labeling: Label Mix-Up; potential for cartons labeled as Tranexamic Acid...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 17, 2020· Maison Terre, LLC

Recalled Item: Goldenseal Root Powder Organic Recalled by Maison Terre, LLC Due to...

The Issue: Microbial Contamination of Non-Sterile Products: FDA laboratory analysis...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 17, 2020· Mylan Institutional LLC

Recalled Item: Tranexamic Acid Injection Recalled by Mylan Institutional LLC Due to...

The Issue: Labeling: Label Mix-Up; potential for cartons labeled as Tranexamic Acid...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 14, 2020· SG24 LLC

Recalled Item: SkinGuard 24 All-Day Hand Sanitizer 2.67 oz. bottle with foam pump Recalled...

The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 14, 2020· SG24 LLC

Recalled Item: Skin Guard 24 All-Day Hand Sanitizer 10 mL Pocket Pen Dist by: SG24 LLC...

The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...

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

Class I — Serious Health HazardOngoing
Refund