State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mars Retail Group is recalling M&M's-branded jewelry due to high lead levels. Consumers should stop using the items and return them for a refund.
J.D. North America is recalling All Power portable gasoline generators because the fuel tank can leak, posing explosion, fire, and burn hazards.
Bison Coach is recalling 654 model year 2015-2016 horse trailers because a missing inline fuse on the battery cable could cause overheating and fire during an electrical short.
Cree is recalling LED T8 replacement lamps that can overheat and melt, posing a burn hazard. No injuries have been reported.
Seagrave is recalling 28 Marauder II fire trucks because a transmission component may fail, preventing the vehicle from pumping water at fire scenes.
Baxter Healthcare is recalling VASCU-GUARD Peripheral Vascular Patches due to postmarketing reports of intraoperative and postoperative bleeding, including one fatal outcome.
Oregon Potato Company is voluntarily recalling specific lots of frozen yellow onion dice due to potential Listeria monocytogenes contamination.
Oregon Potato Company is voluntarily recalling IQF 1/4" Frozen White Onion Dice due to potential Listeria monocytogenes contamination.
Oregon Potato Company is voluntarily recalling specific lots of frozen yellow onion dice due to potential Listeria monocytogenes contamination.
Oregon Potato Company is voluntarily recalling fresh white onion dice due to potential Listeria monocytogenes contamination. The product was distributed across multiple US states, Canada, and Ireland.
Oregon Potato Company is voluntarily recalling 3/8" Frozen Yellow Onion Dice due to potential Listeria monocytogenes contamination. The product was distributed in 17 US states, Canada, and Ireland.
Oregon Potato Company is voluntarily recalling IQF 3/4" Yellow Onion Dice due to potential Listeria monocytogenes contamination.
Golden State Medical Supply Inc. is recalling specific lots of Venlafaxine Hydrochloride Extended-Release Capsules, 150 mg, due to failed dissolution specifications.
Medtronic is recalling Valleylab Laparoscopic Flat L-Hook Electrodes due to a potential sterile barrier breach. The recall covers 119,770 units distributed worldwide.
Oregon Potato Company is voluntarily recalling IQF 3/8" Un-Blanched Yellow Onion Dice due to potential Listeria monocytogenes contamination.
Newly Weds Foods Inc is recalling bulk flour bland breader contaminated with E. coli O121. The product was distributed nationwide in 15, 30, and 50 lb bags or boxes.
Medtronic is recalling Valleylab Laparoscopic Wire L-Hook Electrodes due to a potential sterile barrier breach. The recall covers 50,055 units distributed worldwide.
Oregon Potato Company is voluntarily recalling specific lots of frozen yellow onion strips due to potential Listeria monocytogenes contamination.
Oregon Potato Company is voluntarily recalling fresh white onion strips due to potential Listeria monocytogenes contamination.
Medtronic is recalling 3,470 Valleylab Laparoscopic Flat L-Hook Electrodes because the package may be compromised, potentially breaching the sterile barrier.
Medtronic is recalling 1,440 Valleylab Laparoscopic Wire J-Hook Electrodes because the packaging may be compromised, potentially breaching the sterile barrier.
Synthes (USA) Products LLC is voluntarily recalling 182 units of Titanium Single Vector Distractor Bodies because the fastener may separate prematurely from the Proximal Foot Plate.
Synthes (USA) Products LLC is voluntarily recalling 90 units of Titanium Single Vector Distractor Bodies because the fastener may separate prematurely from the Proximal Foot Plate.
Hyundai is recalling specific 2016 Sonata vehicles because the driver-side frontal air bag may not adequately protect the driver's neck in a crash.
Medtronic is recalling 19,200 Valleylab Laparoscopic Flexible Argon Electrodes because the packaging may be compromised, potentially breaching the sterile barrier.