State
72,936 recalls have nationwide distribution and so reach Tennessee. 7,819 additional recalls listed Tennessee specifically in their distribution scope.
Of the 7,819 recalls naming Tennessee we have scored against our rubric, 1,317 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,653 (21%) are Severe.
Which agencies issued them
These figures cover only the 7,819 recalls whose distribution notice names Tennessee specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Cpzzkq baby loungers are recalled because they violate the mandatory safety standard for infant support cushions and the padding can obstruct an infant's breathing.
TOETOL HOME children's tower stools are recalled because they can collapse or tip over and a child's torso can fit through the side openings. 18 collapses and 11 injuries reported.
Sweetie Baby and Style Life Eleven baby loungers are recalled because their sides are below the minimum height and they have no stand, posing a fall hazard to infants.
KMUYSL Big Red Barn Farm Animal Playsets are recalled because the fence handles can detach from a toy intended for children under three, violating the small parts ban.
mGanna sodium hydroxide pellet bags sold on Amazon by Archie Xpress are recalled because the packaging is not child-resistant, risking chemical burns to skin and eyes.
Jaguar Land Rover North America is recalling certain 2026 Land Rover Defender vehicles because the fuel tank was improperly manufactured with walls that are too thin, which may leak fuel in a crash and increase fire risk.
BlissfulDestiny is recalling its Magnetic Stick Figure Sets because they contain loose magnets that pose a serious injury or death risk if swallowed.
Autobrush Sonic Pro Kids toothbrush delivery boxes are recalled because they contain a lithium coin battery that can be easily accessed by children, posing an ingestion hazard.
Wiifo children's tower stools are recalled because they can collapse or tip over and a child's torso can fit through the side openings. 22 incidents and six injuries reported.
General Motors is recalling specific lots of ACDelco GMW DOT 3 brake fluid that may contain visible sediment, potentially reducing brake performance.
Chrysler is recalling certain Jeep Wagoneer S and Dodge Charger electric vehicles because a software error may cause the instrument panel display to fail, breaching five federal standards.
B. Braun Medical Inc is recalling STREAMLINE BLOODLINE SET FOR DIALOG (Model Number: SL-2010M2096) because air bubbles may accumulate in the arterial line.
B. Braun is recalling StreamLine Bloodline Long Version sets because small air bubbles can accumulate in the arterial line under negative pressure. 328,640 units are affected.
B. Braun is recalling StreamLine Fresenius bloodlines supplied for DaVita because small air bubbles can accumulate in the arterial line under negative pressure. 1,174,271 units are affected.
B. Braun is recalling hemodialysis bloodlines with a 4.8 mm pump segment because small air bubbles can accumulate in the arterial line under negative pressure. 4,884 units are affected.
B. Braun is recalling StreamLine Bloodline Sets for Dialog DR because small air bubbles can accumulate in the arterial line under negative pressure. 3,158,104 units are affected.
Volkswagen is recalling certain 2025-2026 Taos vehicles because the fuel pressure sensor may dislodge from the fuel tank in a rear-end crash, failing FMVSS 301 fuel system integrity.
Toyota is recalling certain 2025 RAV4 vehicles because the front seat brackets for the seat rails may be welded improperly, which can prevent the seat from restraining an occupant in a crash.
Winnebago is recalling certain Ekko motorhomes because the touchscreen may register phantom inputs and start the generator unknowingly, creating a carbon monoxide risk in enclosed spaces.
B. Braun is recalling one model of hemodialysis bloodline because small air bubbles can accumulate in the arterial line when blood gases adhere to the tubing under negative pressure.
Omnipod 5 Pods from 49 lots have an internal soft cannula tear that lets insulin leak inside the Pod instead of being delivered. 1,240,115 units are affected.
Lidocaine HCl Injection, USP 1% in 5 mL single dose vials manufactured by Huons is being recalled for lack of assurance of sterility. All lots within expiry are affected.
Arjo Tenor mobile passive patient lifts are being recalled because an internal actuator component in one production batch may not meet the required mechanical strength.
Cellex Photopheresis Kits are being recalled because the centrifuge bowl is harder to install and, if fitted improperly, may dislodge and break during priming or treatment.
SLMD BP Acne Spot Treatment, 10% benzoyl peroxide, is being recalled because of chemical contamination from the presence of benzene. 2,269 bottles are affected.