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. 2,504 recalls have been distributed to Tennessee in the last 12 months.
Showing 25621–25640 of 29,188 recalls
Recalled Item: 23ga Chow Illuminated Pick Recalled by Synergetics Inc Due to Faulty seals...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC FX 40 instrument Recalled by Becton Dickinson & Co. Due to...
The Issue: Improperly functioning component of a diagnostic medical device may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrocare SPORTS MEDICINE Recalled by ArthroCare Medical Corporation Due to...
The Issue: A sharp edge on the cannulated tip of the device may damage or cut a suture.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap Hi-Line XXS handpiece Hi-Line XXS handpieces are used with Recalled...
The Issue: Certain lots of the Aesculap Hi Line XXS handpiece (part # GB790R) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estrogen Receptor AB-11 (Clone ID5) Mouse Monoclonal Antibody 1 mk Recalled...
The Issue: Reports that the product is not performing as expected. In house testing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRI Low Profile Single Lumen port with Open-Ended 6.6Fr Silicone Recalled by...
The Issue: Bard Access Systems is recalling various Low Profile Port with 6.6 Fr Single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium Single Lumen Low-Profile port Recalled by Bard Access Systems Due...
The Issue: Bard Access Systems is recalling various Low Profile Port with 6.6 Fr Single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catheter Recalled by Merit Medical Systems, Inc. Due to Merit Medical...
The Issue: Merit Medical Systems, Inc. is conducting a recall for 3 lots of Maestro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)...
The Issue: The housing to the Pump's driveline connector became partially or fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Intermittent noise on...
The Issue: Intermittent noise on ECG and/or Respiration waveforms associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMUS Recalled by Siemens Medical Solutions USA, Inc Due to Update to...
The Issue: Update to correct the possibility for patients or operators to have their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Artis Q and Artis Q biplane systems Product Usage: Recalled by...
The Issue: There exists the possibility that during clinical operation, a breakdown of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cusa Excel Rx Only CEM" Nosecone for CUSA¿ Excel Recalled by Integra...
The Issue: The blue COAG button on the CUSA Excel CEM nosecone could stick in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit model 8000 and 8015 with Alaris PCA Recalled by CareFusion...
The Issue: CareFusion is recalling the Alaris PC unit (model 8000 and 8015) because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Intermittent noise on...
The Issue: Intermittent noise on ECG and/or Respiration waveforms associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Essenta DR Recalled by Philips Medical Systems, Inc. Due to X-ray...
The Issue: X-ray system C-arm casting may loosen and fall
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Cyclosporine Flex reagent cartridge an in vitro diagnostic...
The Issue: Complaints were received regarding variability in recovery of QC and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symmetry and CODMAN brands Recalled by Symmetry Medical/SSI Due to The...
The Issue: The Quad-Lock Sterilization Container System may not maintain an effective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed Recalled by...
The Issue: Intermittent noise on ECG and/or Respiration waveforms associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S5/C5 Heart-lung machine Product Usage: The StOckert S5/ Sorin C5 Recalled...
The Issue: Sorin is initiating a field correction on S5/C5 Heart-lung machine and CP5...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.