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. 2,603 recalls have been distributed to Tennessee in the last 12 months.
Showing 16941–16960 of 29,188 recalls
Recalled Item: Brilliance Big Bore (Radiology) - Model no. 728244 Recalled by Philips...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 - Model no. 728323 Recalled by Philips Medical Systems...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 16 Slice (Air) - Model no. 728246 Recalled by Philips Medical...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core - Model no. 728321 Recalled by Philips Medical Systems...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE isp with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GloCyte RBC Reagent - Product Usage: The GloCyte Automated Cell Recalled by...
The Issue: RBC Reagent failure. High fluorescent counts during RBC Reagent + Diluent QC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invia Motion Negative Pressure Wound Therapy System. Labeled as: a. Recalled...
The Issue: Device may display a battery missing error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VOLISTA StandOP Surgical Light Recalled by GETINGE US SALES LLC Due to The...
The Issue: The manufacturer received complaints indicating that the device's central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5" (13 cm) Smallbore Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14 cm (5.5") Appx 0.27 ml Recalled by ICU Medical, Inc. Due to The infusion...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5" (17 cm) Smallbore Ext Set w/Remv MicroClave¿ Clear Recalled by ICU...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due to The infusion...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" Smallbore Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due to The...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5" (17 cm) Appx. 0.57 ml Recalled by ICU Medical, Inc. Due to The infusion...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.