State
73,738 recalls have nationwide distribution and so reach Utah. 4,914 additional recalls listed Utah specifically in their distribution scope.
Of the 4,914 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 1,350 (27%) are Severe.
Which agencies issued them
These figures cover only the 4,914 recalls whose distribution notice names Utah specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Joyson is recalling certain rear seat belt retractors because the locking mechanism may not properly restrain occupants, increasing injury risk in a crash.
Concession Nation is recalling 2019-2020 QUAT trailers because the tire and loading information sticker may display incorrect cargo weight, potentially leading to overloading.
RH is recalling about 800 Camino floor lamps sold in the U.S. because the foot switch can overheat or catch fire, posing a fire hazard.
Joules USA is recalling specific children's pajamas and robes because they violate federal flammability standards, posing a burn hazard to children.
ECHO and Shindaiwa are recalling about 67,700 backpack blowers and 6,600 replacement straps because parts can be expelled, posing laceration and impact risks.
IKEA is recalling KULLEN 3-drawer chests because unanchored units pose tip-over and entrapment hazards that may result in death or serious injuries to children.
Taro Pharmaceuticals is recalling two lots of Phenytoin Oral Suspension because the medication may coagulate and fail to resuspend as directed.
Halcore Group is recalling 2018 AEV Traumahawk ambulances because an undersized power cord may cause an electrical short circuit, increasing the risk of fire or shock.
PACCAR is recalling 2016-2020 Peterbilt 320 and 520 trucks because a missing quick release valve may delay brake release, increasing crash risk.
PACCAR is recalling 2015-2020 Peterbilt trucks because a battery cable may chafe and cause an electrical short circuit, increasing fire risk.
Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they may produce incorrect rotation and margin contour misalignment in scanned data.
Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data during scanning.
Lotte Choco Pie Banana is being recalled because FDA testing found undeclared almond protein. Consumers with this product should stop eating it.
Lotte International America is recalling Lotte Choco Pie Cocao because FDA testing found undeclared almond protein in the product.
Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they may produce incorrect rotation and margin contour misalignment in dental impressions.
Biomet 3i, LLC is recalling specific Bellatek Encode Healing Abutments because they may produce incorrect rotation and margin contour misalignment in dental impressions.
Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour misalignment in dental impressions.
Halcore Group is recalling 2016-2019 Horton Type I and III ambulances because an undersized A/C power cord may cause an electrical short circuit, increasing the risk of fire or shock.
Biomet 3i, LLC is recalling specific Bellatek Encode Healing Abutments because they may produce incorrect rotation or margin contour misalignment in dental impressions.
Zimmer Surgical Inc is recalling 58 units of sterile tourniquet cuffs because a leak between bladders may cause both to inflate or deflate simultaneously.
Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they may cause incorrect rotation and margin misalignment.
Zimmer Biomet is recalling 1,662 units of the THP Hip Plating System after internal testing detected a potential increase in fracture rate and packaging discoloration.
Breas Medical is recalling 629 Vivo ventilator protective covers because the design may obstruct the exhalation valve control pressure tube.
Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data.
Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data during scanning.