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. 1,111 recalls have been distributed to Kentucky in the last 12 months.
Showing 2621–2640 of 13,398 recalls
Recalled Item: Alcohol Swabsticks Recalled by Mckesson Medical-Surgical Inc. Corporate...
The Issue: CGMP Deviations: products were stored outside the drug label specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrogen Peroxide Topical Solution USP Recalled by Vi-Jon, LLC Due to Cross...
The Issue: Cross Contamination With Other Products: Product is cross contaminated with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Capsules Recalled by Loud Muscle Science Due to Marketed...
The Issue: Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Euphoria Capsules Recalled by Loud Muscle Science Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Euphoria Capsules Recalled by Loud Muscle Science Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Capsules Recalled by Loud Muscle Science Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Aphrodisia Capsules Recalled by Loud Muscle Science Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Aphrodisia Capsules Recalled by Loud Muscle Science Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Divalproex Sodium Delayed-Release Tablets Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: Failure occurred during routine stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrogen Peroxide Topical Solution Recalled by Vi-Jon, LLC Due to Labeling:...
The Issue: Labeling: Label Mix-Up-The primary label on the front of the bottles have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours...
The Issue: Defective Delivery System: Customer complaints received for ripping patches...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GOOD SENSE OMEPRAZOLE TABLET 14CT SKU 900055 PRILOSEC OTC TABLET Recalled by...
The Issue: CGMP Deviations: product held outside appropriate storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VASELINE ECZEMA CALMING THERPY CRM 6.8 OZ distributed to specific Recalled...
The Issue: CGMP Deviations: product held outside appropriate storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MYLICON INFANT GAS DROPS 0.5 OZ distributed to specific Family Recalled by...
The Issue: CGMP Deviations: product held outside appropriate storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLARITIN ALLERGY LIQ CHLDRNS GRAPE 2 FLOZ SKU 900834 CLARITIN Recalled by...
The Issue: CGMP Deviations: product held outside appropriate storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DAYQUIL COLD FLU LQD 12 FL OZ SKU 900205 RIC Recalled by Family Dollar...
The Issue: CGMP Deviations: product held outside appropriate storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ORAJEL NON MED TEETHING GEL 0.125 OZ distributed to specific Recalled by...
The Issue: CGMP Deviations: product held outside appropriate storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FS CLOTRIMAZOLE ANTI FUNGAL CREAM .5 OZ distributed to specific Recalled by...
The Issue: CGMP Deviations: product held outside appropriate storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: READY IN CASE PAIN RELIEVER PM CAPLET 100 CT SKU Recalled by Family Dollar...
The Issue: CGMP Deviations: product held outside appropriate storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZARBEES NTRLS BABY CGH MUCUS GRP 2 FL OZ distributed Recalled by Family...
The Issue: CGMP Deviations: product held outside appropriate storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.