State
73,833 recalls have nationwide distribution and so reach Tennessee. 7,861 additional recalls listed Tennessee specifically in their distribution scope.
Of the 7,861 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 7,861 recalls whose distribution notice names Tennessee specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Thor Motor Coach is recalling 2014-2016 Tuscany motor homes because the brake signal to towed devices may not deactivate, causing dragging brakes and fire risk.
GE Healthcare is recalling 97 MSK 1.5T Extreme MR Scanners because gas venting may not occur properly, posing a risk of oxygen deprivation.
Brown & Haley Inc. is recalling Mountain Thins Trail Mix flavor due to potential Listeria monocytogenes contamination.
Hill-Rom is recalling Liko Universal SlingBars because the center bolt may weaken and break, posing a risk of patient falls and injury.
Novacare, LLC is recalling Black Widow 25 Ephedra Super Potent Fat Burner because FDA sampling confirmed the presence of salicylic acid in the product.
Novacare, LLC is recalling Methyldrene Original 25 Ephedra ECA Stack dietary supplements because FDA sampling confirmed the presence of salicylic acid, an unapproved drug.
Novacare, LLC is recalling Thin and Slim Fataway Ultimate Stack with Chromium because FDA sampling found unapproved salicylic acid in the dietary supplement.
Novacare, LLC is recalling Thin and Slim Extreme Stack Fat Burner dietary supplements because FDA sampling confirmed the presence of salicylic acid.
Novacare, LLC is recalling Xcellerator dietary supplements because FDA sampling confirmed the presence of salicylic acid in products marketed without an approved NDA/ANDA.
GE Healthcare is recalling 101 Optima 1.5T MR430s MR Scanners because gas venting may not occur properly, posing a risk of oxygen deprivation.
Publix Super Markets is recalling Cranberry Nut & Seed Mix due to possible Listeria monocytogenes contamination. The product was distributed in six southeastern states.
Frontier Natural Products CO-OP is recalling specific lots of Hojicha Tea due to potential Salmonella contamination. Consumers should stop using the affected products.
Baxter Healthcare is voluntarily recalling Actifuse ABX and MIS System bone void fillers because they may contain endotoxin levels above specification criteria.
GE Healthcare is recalling Revolution CT Patient Tables because the cradle can descend on its own, posing a crushing risk to large patients.
Synthes (USA) Products LLC is recalling 244 DePuy Synthes 8.0 mm Flexible Shaft Reamers because they failed biological safety evaluations for cytotoxicity.
Zimmer Biomet is recalling specific Persona Trabecular Metal Tibial Plate Instruments and Modular Brackets due to incidents of radiolucent lines and loosening in implants.
Berchtold Corp. is recalling 227 HybriGel surgical table cushions because they may contain staples that could appear on patient x-rays.
Becton Dickinson is recalling 811,200 units of 10 mL syringes due to possible adulteration and non-conforming manufacturing practices.
Mercedes-Benz is recalling 2016 C300 4Matic vehicles because a software error may cause the electric power steering assist system to shut down, increasing crash risk.
Sedecal USA is recalling 145 mobile x-ray systems in the US due to a software defect that may apply adult exposure parameters to newborns.
Becton Dickinson is recalling 176,000 units of 10 mL syringes due to possible adulteration and non-conforming manufacturing practices.
Mercedes-Benz is recalling certain 2016 SLK and SL models because low-beam headlights may be aimed incorrectly, potentially reducing driver visibility.
Sony is recalling Panasonic lithium-ion battery packs for VAIO laptops because they can overheat, posing burn and fire hazards. No injuries have been reported.
Nissan is recalling specific 2016 Leaf and Sentra vehicles because a wiring harness connector may disconnect, preventing the passenger air bag from deploying in a crash.
Novo Nordisk is recalling 723 Norditropin FlexPro pens due to a potential assembly fault that may cause the pen to block during the air shot step.