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. 2,661 recalls have been distributed to Tennessee in the last 12 months.
Showing 11321–11340 of 29,188 recalls
Recalled Item: Covidien Best Practices Procedure Kits containing Auto Suture Endo GIA...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker IsoAir 2.0 support surface-provides pressure redistribution and is...
The Issue: Connector between support surface and pump may be out of tolerance resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Loading Unit 45 mm - 2.5mm Recalled by...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Gray Universal Articulating Loading Unit 30 mm - 2.0 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 2.0 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Loading Unit Recalled by Covidien, LP Due to...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 60 mm - 3.5 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 2.5 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 3.5 mm...
The Issue: The device staples may not properly form upon application preventing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactate Dehydrognease P-L Recalled by Randox Laboratories Ltd. Due to An...
The Issue: An update to the carryover avoidance technical bulletin to introduce...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactate Dehydrogenase L-P Recalled by Randox Laboratories Ltd. Due to An...
The Issue: An update to the carryover avoidance technical bulletin to introduce...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tosoh Bioscience AIA-PACK BHCG Calibration Verification Test Set-In Vitro...
The Issue: Decreased stability for five (5) lots of Calibrator Sets and Calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet/Getinge Rotaflow System Console US (115 V / 60 Hz) Recalled by Maquet...
The Issue: Instruction For Use (IFU) incorrect serial number of 90437000. It should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tosoh Bioscience AIA- PACK HCG Calibrator Set-In Vitro Diagnostic for...
The Issue: Decreased stability for five (5) lots of Calibrator Sets and Calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accelerator a3600 system with Sysmex XN-9000/XN-9100 Interface Module (dual...
The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptio Automation systems with Sysmex XN-9000/XN-9100 Interface Module (dual...
The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WallFlexTM Biliary RX Fully Covered Stent System RMV (10mmx60mm Stent)...
The Issue: Mislabeled: WallFlex Biliary RX Uncovered Stent System 10x60mm devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexLab (FLX) with Sysmex XN-9000/XN-9100 Interface Module (dual robot)...
The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is...
The Issue: Potential sterility issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PC Application Software c4D as part of the device Catalyst: Recalled by...
The Issue: PC Application Software c4D not changing Site upon synchronization during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.