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. 1,865 recalls have been distributed to Kentucky in the last 12 months.
Showing 26941–26960 of 51,386 recalls
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Multiple products marketed...
The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Southwestern Gourmet Prickly Pear Popcorn Grand Canyon Foods Recalled by...
The Issue: An FDA inspection revealed products that contained Yellow 5 and soy lecithin...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Alaris Pump Recalled by CareFusion 303, Inc. Due to The bezel manufacturing...
The Issue: The bezel manufacturing process for the FR-110 plastic may have resulted in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin PCS Programmer software model 3330 Recalled by St Jude Medical,...
The Issue: Devices inappropriately displayed a low battery indicator determined to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calendula Cream Recalled by Boiron Inc. Due to Labeling: Labeling Error on...
The Issue: Labeling: Labeling Error on Declared Strength; The outer carton (secondary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CSI Recalled by Cardiovascular Systems Inc Due to The pumps may switch to...
The Issue: The pumps may switch to stand-by during use requiring the pump to be reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Infusion Pump Recalled by Smiths Medical ASD Inc. Due to...
The Issue: Certain Barrel Clamp Guides may contain a ridge that could potentially lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rhino 69 Extreme 50000 packaged in 1 capsule per blister pack Recalled by...
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.
Recalled Item: Morphine Sulfate 2 mg/mL PF Injection. 1 mL in a Recalled by Premier...
The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate 4 mg/mL PF Injection. 1 mL in a Recalled by Premier...
The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone HCl 1 mg/mL PF INJ. 1mL in a 3mL Recalled by Premier Pharmacy...
The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NEOstigmine Methylsulfate (1 mg/mL) 3mg per 3mL. 3mL Single Dose Recalled by...
The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cold Smoked Wild Coho Salmon Lox Recalled by Seabear Company Due to Mislabeling
The Issue: Products recalled due to water phase salt deviations and mislabeling of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hot Smoked Keta Beergarden Salmon Recalled by Seabear Company Due to Mislabeling
The Issue: Products recalled due to water phase salt deviations and mislabeling of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ARROW PICC Set Recalled by Arrow International Inc Due to Product sterility...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPS Rhythm ECG Accessory Pack Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TheraCath(R) Epidural Catheter Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximal Barrier Drape Recalled by Arrow International Inc Due to Product...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7Fr. Catheter Clamp with Fastener Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Echogenic Needle Recalled by Arrow International Inc Due to Product...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.