State
73,809 recalls have nationwide distribution and so reach Tennessee. 7,860 additional recalls listed Tennessee specifically in their distribution scope.
Of the 7,860 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 1,974 (25%) are Severe.
Which agencies issued them
These figures cover only the 7,860 recalls whose distribution notice names Tennessee specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Volkswagen is recalling 2018-2019 Atlas, 2015 Golf SportWagen, and 2019 Jetta vehicles because rear coil springs may fracture, potentially causing loss of control.
Mercedes-Benz is recalling 2019 C300 and AMG C43 vehicles because a software defect may prevent the electronic parking brake from disengaging.
Mercedes-Benz is recalling 2018-2019 S-Class vehicles because the hands-off detection system may fail, keeping steering assist active without driver input.
Feast Mode Blending & Filling is recalling 5,000 units of Garlic Beer Seasoning because the product is mislabeled as 'Gluten Free'.
BMW is recalling 2019 X5 xDrive40i and xDrive50i vehicles because the sun visors may lack required air bag warning labels, increasing injury risk in crashes.
Neotract is recalling UroLift System devices because the capsular tab may fail to deploy, potentially delaying or preventing treatment completion.
Mercedes-Benz is recalling 2018-2019 GLA 250 vehicles because sunroof bonding may allow water leaks that could prevent the window air bag from deploying.
Manhattan Toy is recalling 'Find the Bear' soft books because a metal grommet can detach, posing a choking hazard to young children.
GE Healthcare is recalling 6,458 B20i patient monitors worldwide because network configuration issues may cause the devices to restart unexpectedly.
Heartware, Inc. is recalling 2,031 HVAD System Battery Charger units because they were manufactured with incorrect inductors. The recall covers units distributed in the US and multiple international countries.
Schwan's is recalling Sea Salt Caramel Cashew Ice Cream due to potential glass contamination. Consumers should check production codes and stop using the product.
Nissan is recalling 2015-2017 Altima vehicles because a rear door latch-lock cable may interfere with the window regulator, causing the door to open unexpectedly.
GE Healthcare is recalling 6,864 B40i patient monitors worldwide because network configuration issues may cause the devices to restart unexpectedly.
Howmedica Osteonics Corp. is recalling 28,461 Tritanium Posterior Lumbar cage implants because of reports of fractures occurring during or after surgery.
Dennis Eagle is recalling 2017-2018 Elite refuse trucks because the reverse alarm mute switch can prevent the vehicle from beeping in reverse, increasing injury risk.
GE Healthcare is recalling 33,065 PROCARE B40 patient monitors because network configuration issues may cause the devices to restart unexpectedly.
Gemini Food Corporation is recalling Imperial Taste Fried Red Onion because an investigation found undeclared wheat in the ingredients.
Mercedes-Benz is recalling 2018 S-Class and AMG S63 vehicles because an incorrect steering boot installation may keep the Active Steering Assist system engaged while the driver's hands are off the wheel.
Mercedes-Benz is recalling 2,364 2018 C300 and C300 4MATIC vehicles because improperly adjusted headlights may reduce driver visibility and increase crash risk.
Gemini Food Corporation is recalling Imperial Taste Fried Garlic due to undeclared wheat. The product is distributed in multiple states.
Mercedes-Benz is recalling 2019 CLS 450 and AMG CLS53 vehicles because unsealed headlight adjustment screws may cause improper alignment, increasing crash risk.
Toyota is recalling 2019 Tundra trucks with spray-in bed liners because incorrect load capacity labels may lead to overloading and increased crash risk.
GE Healthcare is recalling 28,004 PROCARE B20 patient monitors because network configuration issues may cause the devices to restart unexpectedly.
GE Healthcare is recalling 5,516 B105/125 patient monitors worldwide because network configuration issues may cause the devices to restart unexpectedly.
Philips is recalling 1,880 HeartStart MRx lithium-ion batteries because a defective component may prevent the battery from charging or delivering power to the monitor/defibrillator.