Product Recalls in Tennessee
Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,670 recalls have been distributed to Tennessee in the last 12 months.
Showing 8801–8820 of 29,188 recalls
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: greiner bio-one VACUETTE TUBE Recalled by Greiner Bio-One North America,...
The Issue: Some of the blood collection tubes show clotting due to variation of Lithium...
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.
Recalled Item: GLOBAL UNITE STD STEM SZ 14 Product Code: 110014100 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 6 Part Number: 11000610 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 8 Part Number: 110008100 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: Medtronic HawkOne Directional Atherectomy System Recalled by ev3 Inc. Due to...
The Issue: Reports have been received of tip damage during use of the devices which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HawkOne Directional Atherectomy System Recalled by ev3 Inc. Due to...
The Issue: Reports have been received of tip damage during use of the devices which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.