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. 2,509 recalls have been distributed to Tennessee in the last 12 months.
Showing 25261–25280 of 29,188 recalls
Recalled Item: MEVION S250 Recalled by Mevion Medical Systems, Inc. Due to Geometric...
The Issue: Geometric positioning error can occur after a rotational correction has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FAS-LOC 6 Foot Disposable Extension Cable with Safe Connect/Screw Down....
The Issue: Remington Medical discovered an error on the FL-601-97 IFU; part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbia T and Symbia T2 computer tomography systems. These systems Recalled...
The Issue: There are confirmed reports of a component coming loose inside the CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Oxylog 3000 plus ventilators Recalled by Draeger Medical Systems,...
The Issue: The potentiometers (knobs) for setting the ventilation parameters may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CRBM Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The firm identified a potential for biased carbamazepine (CRBM) results to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fassier-Duval IM Telescopic System. Orthopedic intramedullary rod implant....
The Issue: The outer package label contained the incorrect length of the device. There...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Medical X Series Recalled by ZOLL Medical Corporation Due to...
The Issue: Defibrillator/Pacemaker/Monitor May Latch in a Continuous Device Reset Loop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alfa Wassermann Diagnostic Technologies Recalled by Alfa Wassermann, Inc....
The Issue: Extremely low absorbance readings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DPM 6 Monitor in use with a Multi Parameter Module Recalled by Mindray DS...
The Issue: The MPM included a cardiac ST/Arrhythmia analysis feature which is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alfa Wassermann Diagnostic Technologies Recalled by Alfa Wassermann, Inc....
The Issue: Extremely low absorbance readings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate II System Controller Product Usage: HeartMate II is a Recalled by...
The Issue: Discovery of serious injuries and deaths associated with the process of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate II Implant Kit with Pocket Controller Recalled by Thoratec...
The Issue: Discovery of serious injuries and deaths associated with the process of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate II LVAD Pump and Pock Controller Kit Recalled by Thoratec...
The Issue: Discovery of serious injuries and deaths associated with the process of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sengstaken Tube and Sengstaken-Blakemore Tube. Teleflex product codes 204800...
The Issue: Sterility of the product cannot be guaranteed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heart Mate II Pocket Controllers removed from packaging Product Usage:...
The Issue: Discovery of serious injuries and deaths associated with the process of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...
The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Morph AccessPro Steerable Introducer Recalled by Biocardia, Inc. Due to Firm...
The Issue: Firm discovered the potential for particulates in the inner lumen of Morph...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...
The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Dual-stage Venous Return Cannulae Recalled by Terumo Cardiovascular...
The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...
The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.