State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Blue Moose of Boulder, LLC is recalling 504 units of All-Natural Ciolo Nut-Free Basil Pesto because the product contains undeclared tree nuts.
Alden Optical is recalling 23 units of HP49 Sphere Daily Wear Soft contact lenses because they lack sterility assurance.
Maxey Trailers is recalling 2017-2018 A3X, A5X, and A6X trailers because suspension arms may crack, potentially causing the axle to come loose and increasing crash risk.
Plant Devas Inc. is recalling Blemish Face Care Kits because FDA sampling found excessive and virulent microorganisms.
Plant Devas Inc. is recalling 144 units of Ayurvedic Face Care Kits because FDA testing found excessive numbers of microorganisms.
Alden Optical is recalling specific daily wear soft contact lenses because they lack sterility assurance. Consumers should stop using the affected lenses.
Sagent Pharmaceuticals is recalling 176,410 vials of methylprednisolone sodium succinate injection due to high impurity levels.
Pfizer is recalling 29,680 vials of Hydromorphone Hydrochloride Injection due to confirmed customer complaints of empty or cracked glass containers.
Alden Optical is recalling NovaKone Daily Wear Soft contact lenses because they lack sterility assurance. The recall covers units distributed in the US and Canada.
Smiths Medical ASD Inc. is recalling certain Port-A-Cath II kits that may contain incorrect introducer sizes or locking collars due to misassembly.
Progressive Laboratories is recalling Xenesta Nuvive Women's 90-count bottles due to potential undeclared milk content.
Forest River is recalling 2018 Surveyor trailers because a missing fan in the refrigerator may cause overheating and fire.
Sagent Pharmaceuticals is recalling methylprednisolone sodium succinate for injection vials due to high impurity levels. The affected lots were distributed nationwide.
Progressive Laboratories is recalling Testosterzone dietary supplements because they may contain undeclared milk, a major food allergen.
Plant Devas Inc. is recalling 500 kits of the evanhealy Clay Mask Kit because FDA testing found excessive and virulent microorganisms.
Plant Divas Inc. is recalling Green Tea Clay because FDA testing found excessive and virulent microorganisms in the product.
Progressive Laboratories is recalling Xenesta Nuvive Men dietary supplements because they may contain undeclared milk.
Alden Optical is recalling ASTERA Multifocal Toric Daily Wear Soft contact lenses because they lack sterility assurance. The recall affects units distributed in the US and Canada.
Plant Divas Inc. is recalling French Rose Clay and Moroccan Rhassoul Clay products because FDA testing found excessive numbers of microorganisms.
Alden Optical is recalling HP59 Toric Daily Wear Soft contact lenses because they lack sterility assurance. Consumers should stop using the affected lenses.
Sagent Pharmaceuticals is recalling 205,370 vials of methylprednisolone sodium succinate for injection due to high impurity levels.
Progressive Laboratories is recalling Thyroid Resilience dietary supplements because they may contain undeclared milk. Consumers should stop using the product and return it to the place of purchase.
Zimmer Biomet is recalling 14,461 TunneLoc Tibial Fixation Devices because gamma sterilization testing suggests the sterilization dose may be inadequate.
Ion Beam Applications is recalling three Proteus 235 proton therapy systems because the internal configuration of electrometers and control boards is not checked before each patient treatment.
Alden Optical is recalling Alden Classic 38 Sphere Daily Wear Soft contact lenses because they lack sterility assurance. The recall covers units distributed in the United States and Canada.