State
73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Super Jumper is recalling approximately 23,000 trampolines because welds on the metal railings can fail, posing fall and injury hazards.
Probar LLC is recalling 14,999 bars of PROBAR MEAL Original Trail Mix because they may contain undeclared milk and soy allergens.
Dorel Juvenile Group is recalling about 24,000 inclined infant sleepers, including Eddie Bauer and Disney Baby models, due to safety concerns about inclined sleep products.
Brand Castle LLC is recalling Arctic Chill Chocolate Mint Cookie Mix due to potential E. coli contamination in flour.
The Crystal Spoon Corp. is recalling Top Chef Meals Grilled Bison Burgers due to potential E. coli contamination. Consumers should not eat the product.
Probar LLC is recalling 50,951 Chocolate Coconut meal bars because they may contain undeclared milk and soy allergens.
Probar LLC is recalling 61,849 Peanut Butter Chocolate Chip meal bars because they may contain undeclared milk and soy.
Pharma-Natural Inc. is recalling Workvie Instant Pain Relieving Roll On due to current good manufacturing practice deviations, including lack of process and cleaning validation.
Brand Castle LLC is recalling Hot Cocoa Cookie Mix because a supplier reported potential E. coli contamination in the flour used.
Brand Castle LLC is recalling Billion Dollar Brownie Mix due to potential E. coli contamination in flour. The product was distributed in ten states.
Gordon Laboratories is recalling 277 boxes of MONSEL'S (Ferric Subsulfate) Solution due to microbial contamination and high iron content.
Tris Pharma is recalling 2,550 bottles of Hydrocodone Polistirex and Chlorpheniramine Polistirex Extended-Release Suspension due to high out-of-specification results for active ingredients and preservatives.
Brand Castle LLC is recalling 46 cases of Million Dollar Cookie Mix due to potential E. coli contamination in flour.
Geritrex, LLC is recalling 6,165 bottles of Gericare Diocto Liquid Stool Softener due to cGMP deviations that may result in microbial contamination.
The FDA is recalling PROBAR Meal Wholeberry Blast bars because they may contain undeclared milk and soy ingredients. Consumers should discard affected bars and consult their healthcare provider if allergic.
Brand Castle LLC is recalling Chocolate Mint Chip Cookie Mix due to potential E. coli contamination in flour supplied by a vendor.
Geritrex, LLC is recalling Ritussin DM Double Strength cough syrup due to cGMP deviations that may result in microbial contamination.
BMW is recalling 2018-2019 X3 and 2019 X4 vehicles because improperly welded front seatback frames may fold unexpectedly, increasing injury risk in a crash.
Geritrex, LLC is recalling Preferred Plus Pharmacy Iron Elixir due to cGMP deviations that may result in microbial contamination.
Geritrex, LLC is recalling 5,107 bottles of Ritussin DM Children & Adults due to cGMP deviations that may result in microbial contamination.
Geritrex, LLC is recalling Preferred Plus Dioctyl Liquid Stool Softener due to cGMP deviations that may result in microbial contamination.
Pharma-Natural Inc. is recalling 500 bottles of Double Tussin DM because the product was manufactured with current good manufacturing practice violations.
Geritrex, LLC is recalling Gericare Geri-Tussin DM due to cGMP deviations that may result in microbial contamination.
MORryde is recalling battery trays for Ford F-550 chassis because inadequate welds may allow the tray to detach, creating a road hazard or battery discharge.
Geritrex, LLC is recalling 8,645 bottles of Diphenhydramine Oral Liquid due to cGMP deviations that may result in microbial contamination.