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. 2,645 recalls have been distributed to Tennessee in the last 12 months.
Showing 12661–12680 of 29,188 recalls
Recalled Item: Siemens ARTIS pheno Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: The potential exists for system movement to be permanently blocked by an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or...
The Issue: Monitor/Defibrillator may not deliver a shock after the "Shock" button on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 MONITOR/DEFIBRILLATOR service kits Recalled by Physio-Control,...
The Issue: Monitor/Defibrillator may not deliver a shock after the "Shock" button on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAINLESS STEEL REPROCESSING TRAY Recalled by Intuitive Surgical, Inc. Due...
The Issue: Small but detectable holes in the sterilization wrap used with the firm's 8...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAINLESS STEEL REPROCESSING TRAY Recalled by Intuitive Surgical, Inc. Due...
The Issue: Small but detectable holes in the sterilization wrap used with the firm's 8...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION PS High Flex XLPE size 5-6 9mm Articular Insert Recalled by Smith &...
The Issue: LEGION PS High Flex XLPE Articular Insert was packaged with an incorrect part
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Daytona Plus (with ISE/without ISE) Recalled by Randox Laboratories,...
The Issue: Software version UI2550642107 for the RX Daytona + instrument released to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost GCF Recalled by Philips Medical Systems Gmbh, DMC Due to When...
The Issue: When using the Table Up/Down button, the system may experience Error 80,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost PCF Recalled by Philips Medical Systems Gmbh, DMC Due to When...
The Issue: When using the Table Up/Down button, the system may experience Error 80,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation stand-alone software treatment planning system. Models 4.0...
The Issue: Three issues found: i) The Map ROI options in the ROI list in the Structure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Recalled by Zimmer...
The Issue: Potential issue associated with the instrument -end of the shaft could fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polysorb Braided Absorbable Suture 6/0 18" UNDYED P-10 Recalled by Covidien...
The Issue: There is a potential for packaging integrity issues impacting the humidity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Enzymatic Creatinine (ECREA) reagent Recalled by Siemens...
The Issue: There is a potential for falsely depressed creatinine results for patients...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polysorb Braided Absorbable Suture 6-0 18" UNDYED SS-24 D/A Recalled by...
The Issue: There is a potential for packaging integrity issues impacting the humidity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polysorb Braided Absorbable Suture 0 30" UNDYED HOS-11 Recalled by Covidien...
The Issue: There is a potential for packaging integrity issues impacting the humidity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polysorb Braided Absorbable Suture 2 36" VIOLET GS-24 Recalled by Covidien...
The Issue: There is a potential for packaging integrity issues impacting the humidity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polysorb Braided Absorbable Suture 4/0 30 VIO SC-2 124K Recalled by Covidien...
The Issue: There is a potential for packaging integrity issues impacting the humidity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polysorb Braided Absorbable Suture 3/0 30" UNDYED V-20 Recalled by Covidien...
The Issue: There is a potential for packaging integrity issues impacting the humidity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biosyn Monofilament Absorbable Suture 6/0 30" VIOLET CV-23 Recalled by...
The Issue: There is a potential for packaging integrity issues impacting the humidity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polysorb Braided Absorbable Suture 2/0 30 VIOLET GS-21 Recalled by Covidien...
The Issue: There is a potential for packaging integrity issues impacting the humidity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.