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 11301–11320 of 51,386 recalls
Recalled Item: THE CHAI BOX CHAI CONCENTRATE 16FL OZ/473ML glass bottles Recalled by The...
The Issue: Potential to be contaminated with Clostridium botulinum. Product was tested...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lyons Ready Care Thickened Orange Nectar packaged in combi-bloc multi...
The Issue: Indication of product spoilage
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Imperial Thickened Cranberry Cocktail Nectar packaged in combi-bloc multi...
The Issue: Indication of product spoilage
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lyons Ready Care Thickened Apple Honey Nectar packaged in combi-bloc...
The Issue: Indication of product spoilage
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lyons Ready Care Thickened Sweet Tea with Lemon Nectar packaged Recalled by...
The Issue: Indication of product spoilage
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lyons Ready Care Thickened Cranberry Nectar packaged in combi-bloc multi...
The Issue: Indication of product spoilage
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lyons Ready Care Thickened Apple Juice packaged in combi-bloc multi Recalled...
The Issue: Indication of product spoilage
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lyons Ready Care Thickened Apple Nectar packaged in combi-bloc multi...
The Issue: Indication of product spoilage
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hamilton-C6 Recalled by Hamilton Medical AG Due to Due to a malfunction...
The Issue: Due to a malfunction related to the backlight on the ventilator screen. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model...
The Issue: Due to increase in Li-Ion Battery failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WEB Detachment Controller Recalled by MICROVENTION INC. Due to Detachment...
The Issue: Detachment controller, of an aneurysm embolization system, has an out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GORE CARDIOFORM ASD Occluder. cardiovascular implant. Recalled by W L Gore &...
The Issue: Due to manufacturing records (Release Test Results) indicating "Failed".
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ampicillin for Injection Recalled by Viatris Inc Due to Presence of...
The Issue: Presence of Particulate Matter: A complaint was received for the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifampin Capsules Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Finished product exceeds the 5...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifampin Capsules Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Finished product exceeds the 5...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride...
The Issue: Incorrect Product Formulation: Oxytocin 30 units was added to an IV bag of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vortex MP Port Titanium Low Profile Implanted Port with 5F Recalled by...
The Issue: Printed Instructions for Use (IFU) not shipped with device. The Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens has become aware of three potential software issues with ARTIS pheno...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci X (IS4200) and Xi (IS4000) systems Recalled by Intuitive Surgical,...
The Issue: Inadvertent energy delivery from surgical system instrument if 1) Force...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insulin Pump/Model: MiniMed 630G/ MMT-1715 Recalled by Medtronic MiniMed Due...
The Issue: Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.