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 26041–26060 of 29,188 recalls
Recalled Item: Portex¿ Spinal Tray with Drugs 22g Whitacre/25g Whitacre Recalled by Smiths...
The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex¿ Spinal Tray with Drugs 25g Whitacre Recalled by Smiths Medical ASD,...
The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex¿ Spinal Tray with Drugs 25g Whitacre Recalled by Smiths Medical ASD,...
The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex¿ Saddleblock Tray with Drugs 25g Quincke Recalled by Smiths Medical...
The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Triage¿ TOX Drug Screen Control 1 Product Generic Name: Recalled by...
The Issue: Alere San Diego, Inc. initiated a voluntary recall of Alere Triage TOX Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex¿ Spinal Tray with Drugs 25g Whitacre Recalled by Smiths Medical ASD,...
The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baylis Medical TorFlex Transseptal Guiding Sheath Recalled by Baylis Medical...
The Issue: The TorFlex Transseptal Guiding Sheath Kits are being recalled due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ComboMap Intravascular Flow and Pressure System Recalled by Volcano Corp Due...
The Issue: A limitation in interoperability between the Philips Xper Flex Cardia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5i/s5ix/s5iz/CORE Intravascular Ultrasound Imaging and Pressure...
The Issue: A limitation in interoperability between the Philips Xper Flex Cardia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5/s5x/CORE Mobile Intravascular Ultrasound Imaging and Pressure...
The Issue: A limitation in interoperability between the Philips Xper Flex Cardia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex¿ Saddleblock Tray with Drugs 26g Quincke Recalled by Smiths Medical...
The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex¿ Regional Anesthesia Tray with Drugs Recalled by Smiths Medical ASD,...
The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex¿ Spinal Tray with Drugs 22g/25g Quincke Recalled by Smiths Medical...
The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultima OPCAB System Recalled by Maquet Cardiovascular, LLC Due to MAQUET has...
The Issue: MAQUET has identified a potential issue with the ULTIMA OPCAB (part numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDRAD¿ Stellant CT Injector System with Certegra Workstation Recalled by...
The Issue: The root cause investigation showed that the under-volume hazard can occur...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Vantage Digital Panoramic System delivers high-value features standard...
The Issue: An error was identified in the Real Time Controller (RTC) firmware versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US)...
The Issue: The trial insertion instrument may disassemble during use due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Absorber Original Recalled by GE Healthcare, LLC Due to GE Healthcare...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX 5.2 DB Server (running Oracle 10.1.0.4.0) Recalled by AGFA Corp. Due...
The Issue: System downtime and/or slow performance may result if software in use is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand: The ForeCYTE Breast Health Test Recalled by Atossa Genetics, Inc. Due...
The Issue: Atossa Genetics is recalling ForeCYTE Breast Health Test, Mammary Aspiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.