State
72,940 recalls have nationwide distribution and so reach Utah. 4,901 additional recalls listed Utah specifically in their distribution scope.
Of the 4,901 recalls naming Utah we have scored against our rubric, 524 (11%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,091 (22%) are Severe.
Which agencies issued them
These figures cover only the 4,901 recalls whose distribution notice names Utah specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
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.
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.
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.
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.
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.
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.
Todson is recalling about 40,245 Concord 360 Degree Rechargeable Light-Up Bike Helmets because they fail to meet safety standards, posing a risk of serious head injury or death.
TheKiddoSpace is recalling its Children's Sensory Swing because the flexible fabric can form loops that pose a risk of serious injury or death from strangulation.
TheKiddoSpace is recalling approximately 650 LED soccer hover balls because the battery surface temperature can exceed safety limits, posing a burn risk.
TheKiddoSpace is recalling its Peg Dolls in Cups Toys because the small peg dolls pose a choking hazard to children under three years old.
Sanven Technology is recalling approximately 10,400 Vevor Retractable Baby Gates because they violate safety standards and pose an entrapment risk to children.
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.
Reser's Fine Foods is recalling 298 tubs of tuna salad that were mislabeled with a Molly Kitchen's Chicken Salad lid, leaving fish undeclared.
Olympus is recalling 1,538 Thunderbeat 5 mm surgical devices worldwide due to continued reports of adverse events. The recall affects all units of Model No. TB-0510IC.
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.
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 27,320 labor and delivery convenience kits due to calibration issues with sterilization equipment that may affect the sterility assurance level of the devices.
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 291 units of three burn care convenience kits due to calibration issues with sterilization and packaging equipment that may affect sterility assurance.
Olympus Corporation of the Americas is recalling the Olympus High Flow Insufflation Unit (Model UHI) because a software algorithm issue may cause overpressure events.
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 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.