State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Newmar is recalling 2017 King Aire, Essex, and London Aire motorhomes because the hydraulic entry step controller may allow steps to retract unexpectedly, increasing the risk of injury.
Brookwood Farms is recalling 126,570 pounds of pulled pork products because they contain soy, an undeclared allergen. No illnesses have been reported.
KME is recalling certain Predator aerial emergency vehicles because the water way trolley could separate from the ladder, posing a falling object hazard.
Target is recalling Halloween LED gel clings because they can separate and expose button batteries, posing choking and ingestion risks to children.
Summer Classics is recalling about 800 swivel rocking lounge chairs because the seat bucket can break away from the base, posing a fall hazard. No injuries have been reported.
Entegra is recalling 2016-2017 Cornerstone and Anthem motorhomes because the Tempurpedic Sealy Mattress may burn quickly, violating federal flammability standards.
Mercedes-Benz is recalling 996 S-Class vehicles because improperly adjusted low-beam headlights may reduce driver visibility and increase crash risk.
Cabela's is recalling commercial food dehydrators because defective wiring can cause heat build-up and fire. No injuries have been reported.
Mercedes-Benz is recalling 2,215 GLE vehicles because improperly adjusted low-beam headlights may reduce visibility and increase crash risk.
Forest River is recalling 2017 Cedar Creek trailers because axles were misidentified as having a 7,000-pound capacity when they are only rated for 6,000 pounds.
Makita is recalling about 450 5057KB circular saws because the lower blade guard can malfunction and expose the blade, posing a laceration risk.
Rucker's Wholesale & Service Co. is recalling Uncle Buck's Maple Nut candy because the label fails to list peanuts, a major allergen, as an ingredient.
NatureBox is recalling Dark Cocoa Nom Noms because some bags may contain peanut butter but do not list peanuts on the label.
B. Braun Medical Inc. is recalling 57,408 units of 5% Dextrose Injection USP due to non-sterility caused by fungal contamination from leaking containers.
The Quaker Oats Company is recalling Quaker Quinoa Granola Bars because sunflower kernels used in their production were linked to a Listeria monocytogenes recall.
The Harvard Drug Group is recalling Diocto Liquid stool softener bottles due to positive findings of Burkholderia cepacia contamination.
The Quaker Oats Company is recalling Quaker quinoa granola bars because they were made with sunflower kernels contaminated with Listeria monocytogenes.
Pharmedium Services, LLC is recalling 350 syringes of Heparin Sodium Injection USP because confirmed subpotency and stability data do not support the expiry date.
Leiter's Compounding is recalling Moxifloxacin intravitreal injections because they were produced using recalled filters, raising concerns about sterility.
Rucker's Wholesale & Service Co. is recalling Cabela's Maple Nut candies because the label fails to list peanuts, a major allergen.
Hospira is recalling 4,768 vials of Marcaine 0.5% injection because a glass defect allowed water ingress, compromising sterility and reducing drug potency.
Complete Packaging & Manufacturing is recalling Nature's Power Solutions Acidophilus Blend dietary supplements because they contain undeclared milk, a major food allergen.
Gold Standard Baking is recalling Publix Maple Walnut Strip Danishes due to the presence of small metal shavings.
Pharmedium Services, LLC is recalling specific lots of fentanyl citrate injection because confirmed subpotency and stability data do not support the expiry date.
Hospira is recalling 15 vials of Marcaine 0.25% injection because a glass defect allowed water to enter, compromising sterility and reducing drug potency.