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 1306113080 of 13,398 recalls

DrugJuly 19, 2012· Abbott Laboratories

Recalled Item: Synthroid (levothyroxine sodium) Tablets USP Recalled by Abbott Laboratories...

The Issue: Defective Container: A number of Synthroid bottles have a localized thin...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 19, 2012· Abbott Laboratories

Recalled Item: Synthroid (levothyroxine sodium) Tablets USP Recalled by Abbott Laboratories...

The Issue: Defective Container: A number of Synthroid bottles have a localized thin...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 19, 2012· Abbott Laboratories

Recalled Item: Synthroid (levothyroxine sodium) Tablets USP Recalled by Abbott Laboratories...

The Issue: Defective Container: A number of Synthroid bottles have a localized thin...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 18, 2012· Fougera Pharmaceuticals Inc.

Recalled Item: Fougera Ketoconazole Cream 2% Recalled by Fougera Pharmaceuticals Inc. Due...

The Issue: Failed Impurities/Degradation Specifications: Ketoconazole Cream 2% is the...

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

Class III — Low RiskOngoing
Refund
DrugJuly 18, 2012· LNK International, Inc.

Recalled Item: Walgreens ASPIRIN FREE TENSION HEADACHE Recalled by LNK International, Inc....

The Issue: Incorrect/Undeclared Excipients: The firm recalled specific lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 16, 2012· Coral Rock Man, Inc.

Recalled Item: X-ROCK 3 Day Pill For Men Recalled by Coral Rock Man, Inc. Due to Marketed...

The Issue: Marketed Without an Approved NDA/ANDA: Products tested positive for...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 16, 2012· Coral Rock Man, Inc.

Recalled Item: Z-ROCK All Natural Male Supplement. 1 capsule blister pack Recalled by Coral...

The Issue: Marketed Without an Approved NDA/ANDA: Products tested positive for...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 12, 2012· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...

The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2012· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...

The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 12, 2012· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...

The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2012· Actavis

Recalled Item: Fentanyl Transdermal System Recalled by Actavis Due to Subpotent; some...

The Issue: Subpotent; some patches may not contain fentanyl gel

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...

The Issue: cGMP Deviations; does not meet in process specification requirements

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Thyro-Tab 0.300 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP Deviations;...

The Issue: cGMP Deviations; does not meet in process specification requirements

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Thyro-Tab 0.088 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP Deviations;...

The Issue: cGMP Deviations; does not meet in process specification requirements

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Thyro-Tab 0.125 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP Deviations;...

The Issue: cGMP Deviations; does not meet in process specification requirements

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...

The Issue: cGMP Deviations; does not meet in process specification requirements

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Thyro-Tab 0.112 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP Deviations;...

The Issue: cGMP Deviations; does not meet in process specification requirements

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...

The Issue: cGMP Deviations; does not meet in process specification requirements

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Thyro-Tab 0.050 mg. Recalled by Lloyd Inc. of Iowa Due to cGMP Deviations;...

The Issue: cGMP Deviations; does not meet in process specification requirements

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...

The Issue: cGMP Deviations; does not meet in process specification requirements

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

Class II — Potential Health HazardOngoing
Refund