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. 2,672 recalls have been distributed to Kentucky in the last 12 months.
Showing 661–680 of 51,386 recalls
Recalled Item: Hardware configuration of the BeneVision Central Monitoring System (CMS)...
The Issue: When the Worstation of the BeneVision DMS has a specific hardware...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Molift Product Name: Molift 4-point sling bars (Accessory...
The Issue: A customer experienced that during assembly and load testing of the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number:...
The Issue: A customer experienced that during assembly and load testing of the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Molift Product Name: Molift 2-point sling bars (Accessory...
The Issue: A customer experienced that during assembly and load testing of the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Molift Product Name: Molift Mover 300 Model/Catalog Numbers:...
The Issue: A customer experienced that during assembly and load testing of the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Pressio 2 ICP Monitoring System Recalled by Sophysa Due to Customer...
The Issue: Customer complaints of Pressio monitor rebooting.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sheathes3D Seamless Viral Barrier Recalled by Sheathing Technologies Inc Due...
The Issue: Vaginal/rectal ultrasound probe covers with a viral barrier may have product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE...
The Issue: Ongoing investigations identified additional instances of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name:...
The Issue: Ongoing investigations identified additional instances of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name:...
The Issue: Ongoing investigations identified additional instances of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cinacalcet Hydrochloride Tablets Recalled by Cipla USA, Inc. Due to CGMP...
The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cinacalcet Hydrochloride Tablets Recalled by Cipla USA, Inc. Due to CGMP...
The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cinacalcet Hydrochloride Tablets Recalled by Cipla USA, Inc. Due to CGMP...
The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE Healthcare Carestation anesthesia system Recalled by GE Medical Systems...
The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carestation anesthesia system Recalled by GE Medical Systems...
The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carestation anesthesia system Power Management Board (PMB)...
The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Meijer Steam Distilled Water Recalled by Meijer Inc Due to Floating black...
The Issue: Floating black foreign substance in the product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Alinity ci-series System Control Module (SCM) Recalled by Abbott...
The Issue: Abbott Laboratories is recalling their Alinity ci-series System Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InPen App Recalled by Medtronic MiniMed, Inc. Due to When app is uninstalled...
The Issue: When app is uninstalled and reinstalled, insulin pen software issue causes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCISSORS Recalled by Medline Industries, LP Due to The items may have weak...
The Issue: The items may have weak packaging seals that may result in a breach of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.