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. 2,492 recalls have been distributed to Tennessee in the last 12 months.
Showing 29161–29180 of 29,188 recalls
Recalled Item: 6.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navitrack System - OS Knee Universal Recalled by Orthosoft, Inc. dba Zimmer...
The Issue: Zimmer CAS voluntarily conducted a retrospective recall of the Navitrack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEHC OEC Injection Cable for MedRad Provis V Contrast Injector. Recalled by...
The Issue: GE initiated a correction to the instructions/use due to the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model...
The Issue: Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model...
The Issue: Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various SRI Surgical Disposable Accessory Packs. SRI's Disposable Accessory...
The Issue: Distribution of a product that did not meet specifications. (labeling error)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Precision MPi is an all-digital multipurpose tilt-C x-ray system Recalled...
The Issue: It was discovered that the Remote Touch Panel (RTP) of the GE Precision MPi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navitrack¿ System - OS Knee Universal Recalled by Orthosoft, Inc. dba Zimmer...
The Issue: ZIMMER CAS voluntarily conducted a retrospective recall of the Navitrack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Benchmark XT/LT and Discovery XT Model Numbers: N750-BMK-FS Recalled by...
The Issue: Ventana Medical System is initiating the recall of the BenchMark and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TSX-301A/2 Aquilion One CT System. The TSX-30IAl2 is a whole Recalled by...
The Issue: The SureStart function may not operate in the usual manner, and you may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXCELART Vantage Recalled by Toshiba American Medical Systems Inc Due to The...
The Issue: The status display in the sequence queue window may not change from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straight Impactor - Dorado IBC Recalled by SpineFrontier, Inc. Due to During...
The Issue: During two separate occasions an impactor plate on the handle broke off...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Finger Sensor for Remmers Recorder (Formerly SnoreSat Sleep recorder) To...
The Issue: The outer jacket is receding away from the black sensor prematurely.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PT Link Waterbath Recalled by Dako North America Inc. Due to Dako is...
The Issue: Dako is recalling the PT Link Waterbath because of a possible electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI PET/CT System Recalled by Philips Medical Systems (Cleveland) Inc Due...
The Issue: The reason for this inspection is to determine if the Spindle Block Servo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba CT systems Recalled by Toshiba American Medical Systems Inc Due to...
The Issue: The systems all have a similar table control board. It has been found that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous Ventilator/Continuous Ventilator with Respiratory Mechanics...
The Issue: The power to the Esprit Display's Backlight is interrupted, causing the GUI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HiRes 90K devices with Helix Electrodes Model CI 1400-02H The Recalled by...
The Issue: Advanced Bionics is recalling the the HiRes 90K cochlear implant with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroView 2800 Recalled by GE OEC Medical Systems, Inc Due to Please be aware...
The Issue: Please be aware that this is not a new recall. The firm has taken action;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 9800 Plus Digital Recalled by GE OEC Medical Systems, Inc Due to Please...
The Issue: Please be aware that this is not a new recall. The firm has taken action;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.