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.
Bee Extremely Amazed LLC is recalling SLIM TRIM U Capsules because they contain undeclared sibutramine, a withdrawn drug.
Cantrell Drug Company is recalling 148 syringes of fentanyl citrate injection because the drug was subpotent. The recall is voluntary and nationwide.
The FDA is recalling Zero Xtreme High Performance Fat Burner capsules because testing found unapproved ingredients. Consumers should stop using the product.
Bee Extremely Amazed LLC is recalling Asset BOLD Capsules because they contain undeclared sibutramine and phenolphthalein, making them unapproved drugs.
Bee Extremely Amazed LLC is recalling Jenesis Capsules marketed as a dietary supplement because they contain undeclared sibutramine and phenolphthalein, both withdrawn from the US market for safety reasons.
Bee Extremely Amazed LLC is recalling XCEL Advanced Capsules because they contain undeclared phenolphthalein, a withdrawn ingredient with carcinogenic concerns.
Bee Extremely Amazed LLC is recalling Asset extreme+PLUS Capsules because the product was found to contain undeclared sibutramine, a withdrawn appetite suppressant.
Cantrell Drug Company is recalling 1,652 syringes of fentanyl citrate because the medication was subpotent. The recall is voluntary and nationwide.
Bee Extremely Amazed LLC is recalling EVOLVE BEE POLLEN Capsules nationwide because they contain undeclared sibutramine and phenolphthalein, both withdrawn from the US market for safety reasons.
The Pictsweet Company is recalling Kroger Cajun Style Mirepoix Blend due to possible Listeria monocytogenes contamination in the onions.
The FDA is recalling SlimeX-15 Capsules because they contain undeclared sibutramine, a withdrawn drug. Consumers should stop using the product.
Cantrell Drug Company is recalling 3,853 syringes of Midazolam HCl injection because the drug was subpotent. The recall is voluntary and nationwide.
The Pictsweet Company is recalling specific lots of frozen chopped onions due to possible Listeria monocytogenes contamination. The recall affects Kroger and Pictsweet brands distributed nationwide.
Cantrell Drug Company is recalling 884 syringes of fentanyl citrate injection because the drug was subpotent. The recall is voluntary and nationwide.
The Pictsweet Company is recalling specific lots of frozen seasoning blends due to potential Listeria monocytogenes contamination in the onion ingredients.
Cantrell Drug Company is recalling fentanyl citrate injection syringes because they contain less active drug than labeled.
The Pictsweet Company is recalling Steam'ables Seasoned Summer Vegetables because they contain onions that may be contaminated with Listeria monocytogenes.
Ferrara is recalling 2014-2016 Igniter vehicles because certain power control modules may cause a short circuit, potentially leading to electrical damage, loss of headlights, or fire.
The Pictsweet Company is recalling Pictsweet Steamables Seasoned Spring Vegetables because the onions used in the product were recalled for possible Listeria monocytogenes contamination.
Michael Angelo's Gourmet Foods is recalling frozen shrimp scampi products that may contain undeclared chicken, egg, and soy due to a packaging error.
The Pictsweet Company is recalling frozen three pepper and onion blends sold under Harris Teeter, Kroger, and Pictsweet brands due to potential Listeria monocytogenes contamination.
The Pictsweet Company is recalling Pictsweet Gumbo Vegetables because the onions used in the product were recalled for possible Listeria monocytogenes contamination.
Cantrell Drug Company is recalling 235 syringes of fentanyl citrate injection because the drug was subpotent. The recall is voluntary and nationwide.
Cantrell Drug Company is recalling 1,570 syringes of Midazolam HCl injection because the drug was found to be subpotent. The recall is voluntary and nationwide.
Cantrell Drug Company is recalling specific lots of Atropine Sulfate Injection Solution because the drug was found to be subpotent.