State
73,737 recalls have nationwide distribution and so reach Tennessee. 7,859 additional recalls listed Tennessee specifically in their distribution scope.
Of the 7,859 recalls naming Tennessee we have scored against our rubric, 1,324 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,973 (25%) are Severe.
Which agencies issued them
These figures cover only the 7,859 recalls whose distribution notice names Tennessee specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Nissan is recalling 2,214 2020 Altima S vehicles because specific Continental tires may be over-cured, increasing the risk of a crash.
Toyota is recalling over 1.5 million vehicles because a fuel pump defect may cause the engine to stall while driving, increasing crash risk.
W L Gore is recalling GORE TAG CONFORMABLE Thoracic Stent Grafts because a secondary deployment fiber attachment prevented completion of deployment via the access hatch.
Bausch Health is recalling 35,424 tubes of Hydrocortisone butyrate Cream, 0.1%, because the product was found to be subpotent.
Alliance Outdoor Products is recalling about 3,400 climbing treestands because cable assemblies can separate due to corrosion, posing a fall hazard.
Hadson (Toko) Trading Co., Inc. is recalling Eishindo brand Cup Jelly (Mini) because the product poses a choking hazard.
Volvo is recalling 2001-2003 S60 and S80 vehicles because the driver-side air bag inflator may rupture, sending metal fragments into the vehicle.
Certain 2020-2021 BMW X5, X6, X7, and related models have a front axle support weld that may separate, potentially affecting vehicle handling and control and increasing crash risk.
Boston Scientific is recalling Hurricane RX Biliary Balloon Dilatation Catheters because the black sheath may detach from the shaft. The recall covers 15,062 units in the US and 12,930 internationally.
Philips is recalling 2,202 sterilizable defibrillator paddles because standard periodic checks may fail to detect a specific failure mode in switchless internal models.
Battelle Memorial Institute is recalling 898 N95 respirators decontaminated by its Critical Care Decontamination System. The recall is due to a failure to maintain required condensation levels during the decontamination cycle.
Coulter Ventures is recalling Rogue Home Timers because the lithium-ion battery can overheat and burn, posing a fire hazard.
Pentax of America Inc. is recalling 39 units of the 9372HD Digital Capture system due to a software issue that may copy exam videos to the wrong patient.
Pentax of America Inc is recalling 39 units of the 9310HD Digital Video Capture Module due to a software issue that may copy patient exam videos to the wrong record.
Walker Edison is recalling about 24,000 drawer chests because they are unstable if not anchored, posing tip-over and entrapment hazards to children.
Merge Healthcare is recalling 47 units of Merge LIS software because a defect causes unrelated medications to appear on patient reports.
RTI Surgical is recalling 420 units of Streamline MIS Navigation System Taps because they have experienced binding with other devices.
Foreign Tire Sales, Inc. is recalling 138 Otani OH-306 commercial truck tires with DOT code 0320 because a manufacturing defect may cause the tread to crack.
Smith & Nephew is recalling 143 units of 5.5MM Arthrogarde Hip Access Cannulas because the J Lock feature was manufactured incorrectly, preventing proper locking into irrigation extenders or arthroscopes.
Target is recalling approximately 122,500 Cat & Jack toddler boots because the toggle can detach, posing a choking hazard to children.
W.L. Gore is recalling GORE TAG stent grafts because the delivery catheter could not be withdrawn after implantation.
GE Healthcare is recalling 64 CT scanners worldwide because incorrect settings may cause smudge artifacts that could be mistaken for pathology.
Intuitive Surgical is recalling one da Vinci Xi Endoscope Controller because improper calibration may cause the endoscope tip to reach higher temperatures, potentially leading to thermal tissue injury.
Thor Motor Coach is recalling 2010-2011 Four Winds Montecito motorhomes because a transfer switch may fail due to heat, increasing fire risk.
Philips is recalling 8,942 sterilizable defibrillator paddles because standard checks may miss a specific failure mode. An updated test procedure is available to detect the issue.