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 25041–25060 of 29,188 recalls
Recalled Item: UPGRD PRGM 9734638 ADD AxiEM NAVIGATION Recalled by Medtronic Navigation,...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRAPE 9732722 TUBE STERILE O-ARM 20PK Recalled by Medtronic Navigation, Inc....
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUMOR RES. PACK 9733553 AxiEM S.M. Recalled by Medtronic Navigation, Inc....
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIT Recalled by Medtronic Navigation, Inc. Due to Medtronic Navigation is...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENT PRGM 9734636 ADD FUSION NAV AxiEM Recalled by Medtronic Navigation, Inc....
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOUSE 9732721 STERILE O-ARM 10PK Recalled by Medtronic Navigation, Inc. Due...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gluma Desensitizer Power Gel Product Usage: Usage: This is a Recalled by...
The Issue: The firm discovered that the Gluma Desensitizer Power Gel can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON SC2000 Ultrasound Systems with software version 3.5 (VA35) and...
The Issue: Potential malfunction due to a software issue for ACUSON SC2000 ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON SC2000 Ultrasound Systems with software version 3.5 (VA35) Recalled...
The Issue: Software issues with ACUSON SC2000 ultrasound with software version 3/5...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbia E camera system. Emission Computed Tomography System used to Recalled...
The Issue: Siemens Medical Solutions USA, Inc. has received reports indicating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoswift¿ PGCL [poly (glycolide-co-caprolactone)] Absorbable Surgical...
The Issue: CP Medical, Inc., is recalling one lot of Monoswift PGCL [poly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: e.cam camera system. Emission Computed Tomography System used to detect...
The Issue: Siemens Medical Solutions USA, Inc. has received reports indicating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump model 8100 with software version 9.1.18 and software Recalled by...
The Issue: CareFusion is recalling the Alaris Pump model 8100 version 9.1.18 because it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enaly 1000 BT-12 Ozone Generator Recalled by William C. Domb, D.M.D., A...
The Issue: William Domb is recalling the Enaly 1000 BT-12 Ozone Generator because it is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAMILTON-G5 Ventilator with software versions between V2.00 and V2.31....
The Issue: Ventilation and alarms of a HAMILTON-G5 ventilator can be suppressed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SW-2008 Snuggle Warm Sterile Cardiac Connective Warming Blanket Recalled by...
The Issue: The hose could separate from the blanket.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExploR 7x26mm Modular Radial Stem Recalled by Biomet, Inc. Due to This lot...
The Issue: This lot of the ExploR Modular Radial Stem may be missing the wedge ramp...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap Inc.(AIC) Miethke Ventricular Catheter with Deflector/Miethke Shunt...
The Issue: AIC (USA) received information regarding 3 complaints in which the deflector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch & Lomb Recalled by Bausch & Lomb Inc- Greenville Solutions Plant Due...
The Issue: Out of specification results for one of the two disinfectants.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...
The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.