State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Penobscot McCrum LLC is recalling Medium Battered Jo-Jo Wedges because the product may contain undeclared milk, posing a risk to individuals with milk allergies.
Koogee-Queen Anne, LLC is recalling The Comfy Cow Georgia Butter Pecan Ice Cream due to E. coli and high Coliform Bacteria counts.
New Flyer is recalling 2015-2017 transit buses because the driver's seat belt buckle may be stuck, preventing the belt from latching.
Medtronic is recalling Deep Brain Stimulation lead kits because the depth stop may not secure properly, potentially causing the lead to be placed beyond the intended target.
Koogee-Queen Anne, LLC is recalling 399 pints of The Comfy Cow Double Fold Vanilla Ice Cream due to E. coli and high Coliform Bacteria counts.
Grandma's Herbs is recalling Cholesterol Support dietary supplements because they contain undeclared soy lecithin, a common allergen.
Handi-Craft is recalling Dr. Brown's Natural Bottle & Dish Soap because it may contain harmful bacteria. No injuries have been reported.
Penobscot McCrum LLC is recalling 951 cases of Medium Coated Jo-Jo Wedges because the product may contain undeclared milk.
Lakeside Foods, Inc. is recalling 1,856 cases of IQF green beans in 17 states due to potential Listeria monocytogenes contamination.
Koogee-Queen Anne, LLC is recalling The Comfy Cow Intense Dark Chocolate Ice Cream due to E. coli and high Coliform Bacteria counts.
Medtronic Navigation is recalling 277 reusable ENT suction instruments because they fail pre-use verification checks. The devices are used with the StealthStation AxiEM surgical navigation system.
Penobscot McCrum LLC is recalling 18,799 cases of seasoned baby Jo-Jo wedges because the product may contain undeclared milk.
Alcon is recalling 367 ORA Systems with VerifEye because a software error may cause incorrect intraocular lens power measurements during cataract surgery.
Koogee-Queen Anne, LLC is recalling 53 pints of The Comfy Cow Banana Pudding Y'all Ice Cream due to E. coli and high Coliform Bacteria counts.
Shippert Medical Technologies is recalling Tissu-Trans Filtron 100 units because the seal integrity of the sterile packages cannot be assured.
Penobscot McCrum LLC is recalling Battered Jo-Jo Wedges because the product may contain undeclared milk, posing a risk to individuals with milk allergies.
Koogee-Queen Anne, LLC is recalling The Comfy Cow Cow Trax Ice Cream 1 pint due to E. coli and high Coliform Bacteria counts.
Medtronic is recalling eight AxiEM ENT suction kits because the instruments fail mandatory pre-use verification tests.
Medtronic is recalling 15 Fusion ENT Instrument Kits because the instruments fail pre-use verification. The kits were distributed in the US and Canada.
Penobscot McCrum LLC is recalling 5,782 cases of Medium Seasoned/Battered Jo-Jo Wedges because the product may contain undeclared milk.
Penobscot McCrum LLC is recalling 21,560 cases of Broaster Recipe Crinkle Cut Seasoned Wedges because the product may contain undeclared milk.
C. O. Truxton is recalling specific lots of Phenobarbital Tablets USP, 60 mg, due to a label mixup that may result in mislabeling.
C. O. Truxton is recalling Phenobarbital Tablets USP, 100 mg, due to a label mixup that may result in mislabeled products.
Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 500 because the seal integrity of the sterile packages cannot be assured.
Medtronic is recalling 13 reusable ENT instrument sets because they fail required pre-use verification checks. The devices are used with the StealthStation AxiEM surgical navigation system.