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. 2,634 recalls have been distributed to Kentucky in the last 12 months.
Showing 8901–8920 of 28,748 recalls
Recalled Item: Neuro Convenience Kit Recalled by Medline Industries Inc Due to NaCl 250 mL...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains two...
The Issue: Excessive ultraviolet-C radiation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith and Nephew EVOS Self-Tapping Locking Screw SST: (1) Recalled by Smith...
The Issue: The labels on the packages of screws were switched.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott HeartMate Touch Communication System Recalled by Thoratec Corp. Due...
The Issue: If LVAS communication system is trying to establish Bluetooth connection and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Ocean Water Seal Chest Drain is a plastic Recalled by Atrium Medical...
The Issue: Inadequate/inappropriate Set-Up Instructions, which may result in delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 1.0 and 1.1 multi-functional general R/F system Recalled...
The Issue: If the system experiences an overvoltage / power surge it can cause a short...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system Recalled...
The Issue: If the system experiences an overvoltage / power surge it can cause a short...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iDesign Recalled by AMO Manufacturing USA, LLC Due to Aberrometer and...
The Issue: Aberrometer and precision laser systems are affected by a remote code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalys Precision Laser System Recalled by AMO Manufacturing USA, LLC Due to...
The Issue: Aberrometer and precision laser systems are affected by a remote code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HURRICANE RX DILATION BALLOON 6MM 4CM- -for endoscopic dilatation of...
The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HURRICANE RX DILATION BALLOON 10MM 4CM -for endoscopic dilatation of...
The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HURRICANE RX DILATION BALLOON 10MM 2CM -for endoscopic dilatation of...
The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HURRICANE RX DILATION BALLOON 4MM 4CM-for endoscopic dilatation of...
The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HURRICANE RX DILATION BALLOON 4MM 2CM-for endoscopic dilatation of...
The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HURRICANE RX DILATION BALLOON 8MM 2CM -for endoscopic dilatation of Recalled...
The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HURRICANE RX DILATION BALLOON 8MM 4CM -for endoscopic dilatation of Recalled...
The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HURRICANE RX DILATION BALLOON 6MM 2CM-for endoscopic dilatation of...
The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomeme SARS-CoV-2- Real Time RT-PCR Test Recalled by Biomeme, Inc. Due to...
The Issue: The current IFU specifies a shelf-life of one week after resuspension of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q.zen ceiling with software VD12-angiography systems developed for...
The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q floor with software VD12- angiography systems developed for Recalled...
The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.