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.
Showing 13361–13380 of 13,398 recalls
Recalled Item: buPROPion Hydrochloride Extended-Release Tablets (XL) Recalled by McKesson...
The Issue: Failed USP Dissolution Test Requirements: Possible out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (Methylphenidate) Transdermal System Patch Recalled by Noven...
The Issue: Miscalibrated/Defective Delivery System; exceeded the specification for both...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Balnetar Therapeutic Tar Bath Recalled by Ranbaxy Inc. Due to Subpotent...
The Issue: Subpotent (Single Ingredient Drug): out-of-specification result for coal tar...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Tablets Recalled by Zydus Pharmaceuticals USA Inc...
The Issue: Presence of Foreign Substance(s): A product complaint was received from a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ciprofloxacin Tablets Recalled by Pack Pharmaceuticals Due to Labeling...
The Issue: Labeling Illegible: Missing Label; The voluntary recall of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Northstar Zolpidem Tartrate Tablets USP 10 mg. Manufactured for Northstar RX...
The Issue: Adulterated Presence of Foreign Tablets: This product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc Due to...
The Issue: Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyro-Tab.075 mg. Recalled by Lloyd Inc Due to Subpotent (Single Ingredient...
The Issue: Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hard Ten Days Capsule Recalled by www.vitaminbestbuy.com Due to Marketed...
The Issue: Marketed Without an Approved ANDA/NDA: presence of sildenafil
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Japan Weight Loss Blue Capsules Recalled by www.vitaminbestbuy.com Due to...
The Issue: Marketed Without an Approved ANDA/NDA: presence of sibutramine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Man King Capsules Recalled by www.vitaminbestbuy.com Due to Marketed Without...
The Issue: Marketed Without an Approved ANDA/NDA: presence of sildenafil.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eloxatin (OXALIplatin injection) 5 mg/mL injection Recalled by...
The Issue: CGMP Deviations: Eloxatin was manufactured by Ben Venue Laboratories, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eloxatin (OXALIplatin injection) 5 mg/mL Injection Recalled by...
The Issue: CGMP Deviations: Eloxatin was manufactured by Ben Venue Laboratories, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc Due to...
The Issue: Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyro-Tab 0.050mg. Recalled by Lloyd Inc Due to Subpotent (Single Ingredient...
The Issue: Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Actra-SX 500 Capsules Recalled by Body Basics Inc Due to Marketed without an...
The Issue: Marketed without an Approved NDA/ANDA; product contains sildenafil, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChloraPrep with Tint Recalled by Carefusion 213, Llc Due to Lack of...
The Issue: Lack of Assurance of Sterility: A customer complaint reported some units had...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prefera OB One Gel Capsules Recalled by Meda Pharmaceuticals Inc. Due to...
The Issue: Labeling: Presence of Undeclared Color Additive; The product is being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xactdose Phenytoin Oral Suspension Recalled by VistaPharm, Inc. Due to...
The Issue: Defective container; lidding deformity allows the contained product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Arthrotec 75 (diclofenac sodium and misoprostol) tablets Recalled by...
The Issue: Tablet Separation: The manufacturer of Arthrotec had recalled the lots that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.