State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mylan Institutional is recalling Mirtazapine 45 mg tablets because they may contain foreign Glipizide 10 mg tablets.
Siemens is recalling 35 PRIMUS HI and Mevatron M2 linear accelerators due to a defective weld seam that could cause overhead suspensions to fall and injure people.
Mylan Pharmaceuticals is recalling Mirtazapine tablets because bottles may contain foreign Glipizide 10 mg tablets. Consumers should stop using the product and contact their pharmacist.
Endo Pharmaceuticals is recalling 5,086 cartridges of EDEX (alprostadil) 10mcg injection due to a defective container that compromises sterility assurance.
Siemens Medical Solutions USA is recalling 35 MEVATRON M 6700 linear accelerators due to a defective weld seam that could cause the overhead suspension to fall and injure a patient or other person.
Villa Sistemi Medicali is recalling 65 Apollo EZ x-ray systems because the footrest detached from the table, causing a patient to fall.
Nu Skin is voluntarily recalling Pharmanex ageLOC TR90 Protein Boost because it contains an undeclared milk allergen.
Villa Sistemi Medicali is recalling 65 Apollo DRF x-ray systems because the footrest can detach, causing patients to fall from the table.
Trail King is recalling 2016-2017 ACS and AACS drop deck fifth wheel trailers because the coupler plate may crack, allowing the trailer to detach from the tractor.
Siemens is recalling 35 MEVATRON KD-2 linear accelerators due to defective weld seams that could break and cause the overhead suspension to fall, posing a risk of severe injury.
Siemens is recalling 35 linear accelerator systems due to defective weld seams that could cause overhead suspensions to fall, posing a risk of severe injury.
Versa Marketing is recalling Fusia Asian Aspirations Szechuan Stir Fry because the product tested positive for Listeria monocytogenes. The recall affects 4,089 cases sold at Aldi stores nationwide.
Siemens is recalling 35 MEVATRON M 6730/6740 linear accelerators because defective weld seams on overhead suspensions could break and fall, posing a risk of severe injury.
Siemens is recalling 35 MEVATRON M 7400/7440 linear accelerators because a defective weld seam could break, causing the overhead suspension to fall and potentially injure patients or others.
McCormick & Co. is voluntarily recalling 18oz bottles of Stubb's Sticky Sweet BBQ Sauce due to glass defects that may cause chipped or missing glass.
Siemens is recalling IMMULITE Progesterone test kits because DHEA-S causes falsely elevated results, potentially affecting diagnosis.
Robert Rothschild Farm LLC is recalling Gift Sets with Pretzel Twists because the product is not labeled with an ingredient statement, failing to declare soy and wheat allergens.
Ride The Ducks International LLC is recalling 1996-2014 amphibious vehicles because driver seats and seat belts may not secure occupants in a crash.
Parker Medical is recalling specific lots of Left Double Lumen Endobronchial Tubes because the single lung isolation feature did not function as intended.
The See Clear Company is recalling 119,829 units of color contact lenses because they may not be sterile and may have incorrect lot numbers or expiry dates.
Nu Skin Enterprises is voluntarily recalling Pharmanex Cortitrol capsules because they contain undeclared soy, a major food allergen.
Robert Rothschild Farm LLC is recalling Gift Sets with Chocolate Pretzel Dippers because the product is not labeled with an ingredient statement, failing to declare the allergens soy and wheat.
Siemens is recalling IMMULITE 2000 Progesterone kits because DHEA-S causes falsely elevated results, potentially affecting diagnosis.
Nu Skin Enterprises is voluntarily recalling Pharmanex Cholestin softgels because the product contains undeclared soy, a common allergen.
VanLeigh is recalling 2016-2017 Vilano fifth-wheel trailers because incorrect Federal Placard information may lead to vehicle overloading.