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 8741–8760 of 28,748 recalls
Recalled Item: THERAKOS CELLEX Photopheresis Procedural Kit Recalled by Mallinckrodt...
The Issue: This recall was initiated to recover a Dunnage Case, which is a case of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vaporizer Sevoflurane Maquet Filling Recalled by Getinge Usa Sales Inc Due...
The Issue: A potential chemical degradation of Sevoflurane by Lewis acids (metal oxides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTISTE with syngo RT Therapist-linear accelerator systems to deliver X-Ray...
The Issue: Potential safety issue under specific preconditons that may result in a user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R82 by ETAC Push Brace for High-Low Recalled by R82 A/S Due to The chrome...
The Issue: The chrome surface of the push brace can crack during use, potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Subdermal Needle Electrode Recalled by Technomed Europe Due to...
The Issue: There is a high risk of the blue hub detaching from the corkscrew needle,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novalung Sensor Box (F30000163) a component of Novalung Console (F30000162)-...
The Issue: Error messages 206 (yellow) and 208 (red) technical failure, flow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE REV STEM SZ 10 Product Code: 110010600 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 16 Product Code: 110016100 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 10 Part Number: 110010100 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 12 Product Code: 110012100 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE REV STEM SZ 8 Part Number: 110008600 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.