State
73,809 recalls have nationwide distribution and so reach Utah. 4,916 additional recalls listed Utah specifically in their distribution scope.
Of the 4,916 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 1,351 (27%) are Severe.
Which agencies issued them
These figures cover only the 4,916 recalls whose distribution notice names Utah specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Elekta is recalling 2,998 Digital Accelerators worldwide due to a potential for uncontrolled extension of iViewGT or XVI detector arms.
BSN Sports is recalling rubber critter toys because the orange and yellow paint contains lead levels exceeding federal bans. No injuries have been reported.
Reser's Fine Foods is recalling specific lots of Pasta Spinach with Cavatappi because the spinach ingredient may be contaminated with Cyclospora.
Reser's Fine Foods is recalling Bow Tie Florentine pasta salad because it contains spinach potentially contaminated with Cyclospora. The product is distributed in 12 US states and Canada.
Philips is recalling DigitalDiagnost Dual Detector units because the footplate hook may fail, causing the plate to fall and injure patients or operators.
Philips is recalling DigitalDiagnost 4.1 Flex and Value units because the footplate hook may fail, causing the footplate to fall and injure patients or operators.
GE Healthcare is recalling specific CT systems because a damaged cable may expose 120VAC to service engineers working inside the gantry.
Philips is recalling DigitalDiagnost Upgrades because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Philips is recalling DigitalDiagnost 4.1 Chest X-Ray units because a defective hook allows the footplate to fall, posing a risk of injury to patients or operators.
Philips is recalling EasyDiagnost Eleva DRF units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Philips is recalling DigitalDiagnost Dual Detector units because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Philips is recalling EasyDiagnost Eleva DRF units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Philips is recalling DigitalDiagnost Release 3.1 units because a defective hook allows the footplate to fall or swing, posing an injury risk to operators or patients.
Philips is recalling two DigitalDiagnost 2.x Upgrades because a defective hook allows the footplate to fall or swing, posing a risk of injury to operators or patients.
Zimmer Biomet is recalling 247 connecting bolts made from incorrect material, which may decrease fatigue strength and lead to fracture.
GE Healthcare is recalling Optima CT540 systems because a damaged cable may expose 120VAC to service engineers working inside the gantry.
Philips is recalling DigitalDiagnost Release 3.1 units because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Handicare USA Inc. is recalling 716 C Series Patient Lifts because straps may wear and break prematurely at maximum weight conditions.
Philips is recalling DigitalDiagnost Classic 1.x Upgrades because the footplate hook may fail to hold the plate securely, posing a risk of injury to patients or operators.
CAREstream Medical LLC is recalling 919 ProNox Nitrous Oxide Delivery Systems because two units delivered higher levels of nitrous oxide than specified during routine testing.
Reser's Fine Foods is recalling Bow Tie Pasta Caesar due to potential Cyclospora contamination from spinach ingredients.
Philips is recalling DigitalDiagnost 4.1 High Performance units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Philips is recalling DigitalDiagnost 4.1 units because a defective hook allows the footplate to fall, posing a risk of injury to patients or operators.
Philips is recalling DigitalDiagnost 4 High Performance units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Philips is recalling DigitalDiagnost Single Detector units because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.