State
73,741 recalls have nationwide distribution and so reach Tennessee. 7,859 additional recalls listed Tennessee specifically in their distribution scope.
Of the 7,859 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 1,973 (25%) are Severe.
Which agencies issued them
These figures cover only the 7,859 recalls whose distribution notice names Tennessee specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Baxter Healthcare is recalling Exactamed 5 mL Oral Dispensers because pharmacy packs may contain 10 mL dispensers.
Phadia Ab is recalling 387 Phadia 1000 immunodiagnostic instruments due to a liquid sensor error. The recall affects facilities in 27 US states.
Agilent Technologies is recalling MassHunter Quantitative Analysis Software versions B.07 or below due to a defect that causes sample name mismatches and prevents saving changes.
Bausch & Lomb is recalling specific Laseredge Knives used in ophthalmic surgery because they may have dull edges.
Stryker GmbH is recalling 1,533 Endotrac EPF/EGR Triangle Blades because the sterile bag seal integrity may be compromised, potentially affecting sterility.
Alkermes is recalling 6,514 Vivitrol kits because 1-inch needles were incorrectly placed in sleeves labeled for 1.5-inch needles. The drug vials are not impacted.
Akorn, Inc. is recalling 4,085 vials of Eptifibatide Injection because they failed impurity specifications for D-aspartic acid.
Aurobindo Pharma USA Inc. is recalling 2,352 bottles of 40 mg Simvastatin tablets because some bottles were labeled with the wrong lot number and expiration date.
Akorn, Inc. is recalling Eptifibatide Injection vials because they failed impurity specifications for D-aspartic acid.
Akorn, Inc. is recalling 648 vials of Eptifibatide Injection because the fill volume was below specification and a known impurity exceeded limits.
The Beaufort Bonnet Company is recalling handmade knit dolls because a sewing needle was found in the stuffing, posing a puncture injury risk.
Lion Electric Company is recalling 2018 Lion C electric school buses because loose auxiliary brake pump connectors may cause loss of braking ability if the main pump fails.
RH is recalling about 3,200 children's chairs and stools sold in the U.S. and Canada because the paint contains lead levels exceeding federal bans.
NHTSA is recalling 2020 Coachmen Catalina travel trailers because short fasteners may allow upper sleeping bunks to fall, posing an injury risk.
RH is recalling about 5,400 Ultra-Soft Turkish robes because they fail federal flammability standards, posing a burn risk. Consumers should stop using them and request a refund.
WAYB is recalling Pico child seats manufactured between February and August 2019 because the headrest frame can break and detach, increasing injury risk in a crash.
GreatCall is recalling Lively Mobile Plus emergency alert devices because the call button may fail during an emergency. No injuries have been reported.
Chrysler is recalling 2019-2020 Jeep Cherokee vehicles because the steering rack gear may break, potentially causing a loss of steering control and increasing crash risk.
FCA US is recalling 2020 Jeep Gladiator vehicles because rear driveshafts may lack grease, risking overheating, seizure, or fracture that could cause a crash.
Ford is recalling 116,160 vehicles because road salt may corrode steering bolts, causing loss of power steering assist and increasing crash risk.
Indian Motorcycle is recalling 2019 Chieftain models because tail lights may be too bright, potentially confusing other drivers and increasing crash risk.
Decathlon USA is recalling about 50 Rocky Screwgate carabiners because incorrect assembly can cause them to unlock while in use, posing a risk of serious injury or death.
Pearhead is recalling Ubbi Connecting Bath Toys because they can break and create sharp points, posing choking and laceration hazards to young children.
FCA US is recalling 2019 Ram 2500 and 3500 trucks because incorrect assembly fluid in brake calipers may cause seals to swell, leading to dragging brakes and increased crash risk.
Sandoz is recalling approximately 636,000 bottles of Losartan Potassium and Ezetimibe because the caps do not meet child-resistant requirements, posing a poisoning risk to children.