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. 2,536 recalls have been distributed to Tennessee in the last 12 months.
Showing 21661–21680 of 29,188 recalls
Recalled Item: MAGNETOM systems Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Possible installation error of the quench lines of superconducting magnets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to Coil overheating...
The Issue: Coil overheating can occur when the device is used in Mode 2 setup. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quick Connects. Steris Corporation. Model numbers: QKC1736E Recalled by...
The Issue: The firm discovered that one of the hysteroscope models listed for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model NuCARTGN. The NuCART is a mobile display and image Recalled by...
The Issue: The attachment of the NuCART Spring Arm to the NuCART horizontal boom may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...
The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...
The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...
The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...
The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...
The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Position Pro Mattress. Mattress Recalled by Stryker Medical Division...
The Issue: Potential for power cord to melt; hazards include electric shock and fire.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gynecare Thermachoice III Uterine Balloon Therapy System Ethicon Recalled by...
The Issue: Stability data does not substantiate the labeled two-year shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS300 radiographic Cassette Holder or Wall Stand. For use in Recalled by Del...
The Issue: The wall stand cassette holder can suddenly fall to the bottom of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS200 radiographic Cassette Holder or Wall Stand. For use in Recalled by Del...
The Issue: The wall stand cassette holder can suddenly fall to the bottom of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo Humidifier 163 Recalled by Teleflex Medical Due to Cracks may occur at...
The Issue: Cracks may occur at the 15mm and 22mm ISO female connector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Model 3500 and 4000 Syringe Infusion Pumps and Medfusion Recalled...
The Issue: There have been intermittent issues with Supercap POST (power on self-test)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Best Practice Kits containing certain production lots of Endo GIA Recalled...
The Issue: Staplers fail to fire or partially fire and reports of the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo GIA Ultra Universal 12 mm XL Stapler Handle Recalled by...
The Issue: Staplers fail to fire or partially fire and reports of the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo GIA Ultra Universal 12 mm Short Stapler Handle Recalled by...
The Issue: Staplers fail to fire or partially fire and reports of the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRN 50-M+ Recalled by Gsi Group Inc Due to The item was recalled due to an...
The Issue: The item was recalled due to an increased user/patient risk of exposure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.