State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Sanven Technology is recalling approximately 10,400 Vevor Retractable Baby Gates because they violate safety standards and pose an entrapment risk to children.
Zelbuck Magnetism Ball Game Toys are being recalled because they contain loose magnets that pose a serious injury or death risk if swallowed.
SumDirect LED Mini Lights are recalled because the button cell batteries can be easily accessed by children, posing an ingestion hazard. No injuries have been reported.
Andersen Windows is recalling about 91,000 window opening control devices sold as kits or installed on 100 Series casement windows because they can break or detach after impact, posing fall and serious injury hazards. No injuries have been reported.
About 81,800 Babysense Max View baby monitors are recalled because the display unit can overheat and spark while charging, creating a fire hazard. Hisense has received 11 incident reports with no injuries reported.
TheKiddoSpace is recalling about 19,700 children's handwriting practice kits because the pens contain lead levels that violate the federal lead content ban. No injuries have been reported.
Magnetic chess games sold on Amazon by Kaiwenshangpin are recalled because loose magnets inside can be swallowed by children, potentially causing intestinal damage or death. No injuries have been reported.
TheKiddoSpace is recalling about 140 children's story books because felt parts can detach and pose a choking hazard. No injuries have been reported.
PQL recalls about 186,520 high bay linear LED light fixtures because degrading retaining pins can cause the LED board to come loose and spark a fire. One fire has been reported with no injuries.
Joyreal Busy Board children's toys are recalled due to choking and laceration hazards from a detachable small mirror with sharp edges. No injuries have been reported.
TheKiddoSpace is recalling about 4,300 reusable water balloons because the cord lock on the storage bag contains a regulated phthalate that violates the federal phthalate ban. No injuries have been reported.
Honda is recalling certain 2024 Acura ZDX and Prologue vehicles because a software error may cause the instrument panel display to fail and the rearview camera to show a blank screen in reverse.
About 150 Bicystar high chairs (model TB-HC6900) sold on Amazon are recalled because they lack the required crotch restraint and can trap a child's head, creating fall and entrapment hazards. No injuries have been reported.
General Motors has recalled multiple Chevrolet, GMC, Cadillac, and Buick vehicles from 2025–2027 because their radios were not properly configured to download the electronic owner's manual during production. Without the manual, owners may not know how to safely operate the vehicle.
Art Monkey LLC is recalling 8,500 bottles of Why Not Natural Moringa Capsules because they have the potential to be contaminated with Salmonella.
Olympus Corporation of the Americas is recalling 744 Olympus High Flow Insufflation Units (Model UHI-2) because a software algorithm issue may cause overpressure events.
Integra LifeSciences is recalling 2,906 units of its Private Label CVS wound dressings (Model CVS405406) due to potential packaging failures that could compromise the sterile barrier.
Olympus is recalling 485 High Flow Insufflation Units (Model UHI-3) nationwide due to a software algorithm issue that may cause dangerous overpressure during abdominal surgery.
Medline is recalling 753 units of its tracheostomy convenience kits and trach tote due to potential sterilization equipment calibration issues that may affect the sterility assurance level of the devices.
Medline is recalling 291 units of three burn care convenience kits due to calibration issues with sterilization and packaging equipment that may affect sterility assurance.
Medline is recalling 12,418 units of various surgical convenience kits due to calibration issues with equipment used for sterilization and packaging, which may affect the sterility assurance level of the devices.
Medline is recalling 4,757 units of convenience surgical kits distributed worldwide due to calibration issues with sterilization and packaging equipment that may affect sterility assurance.
Medline is recalling 448 units of its BASIC NERVE BLOCK TRAY W/LINEN (Model PAIN0150C) due to calibration issues with sterilization and packaging equipment that could affect the sterility assurance level of the devices.
Medline is recalling 27,320 labor and delivery convenience kits due to calibration issues with sterilization equipment that may affect the sterility assurance level of the devices.
Olympus is recalling 9,542 Thunderbeat surgical devices worldwide due to continued reports of adverse events. The recall affects all lots of the TB-0545FCS model.