State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Dr. Reddy's Laboratories is recalling Zenatane (isotretinoin) capsules because some lots failed to meet dissolution specifications.
Cook Medical is voluntarily recalling 335 LapSac Introducer Sets because the provided reprocessing instructions lack sufficient detail for proper cleaning, disinfection, and sterilization.
Cook Medical is voluntarily recalling Willscher Vas Reapproximator Plates because the reprocessing instructions lack sufficient detail for cleaning, disinfection, and sterilization.
Qualgen is recalling Estradiol 10 mg pellets due to CGMP deviations and lack of quality assurance. The recall covers 5,260 pellets distributed nationwide.
Qualgen is recalling Estradiol 20 mg pellets due to CGMP deviations and lack of quality assurance. The recall covers 4,468 pellets distributed nationwide.
Argon Medical Devices is recalling specific arterial access needles due to a potential packaging defect involving unsealed pouches.
Medtest Holdings, Inc. is recalling MedTest DX Assayed Human Multi Sera Control Level 1 and Level 2 because control values are outside of specification.
Hetero USA Inc. is recalling 13,692 bottles of Acyclovir 800 mg tablets because human hair was found melded into the tablets.
OFD Foods is recalling Mountain House freeze-dried beef hash due to possible rubber contamination. No illnesses have been reported.
Chrysler is recalling 2011-2012 Dodge Grand Caravan vehicles because the driver's air bag wiring may chafe and short circuit, causing unexpected deployment.
Trango is recalling about 2,600 Vergo belay devices because the handle can loosen, causing the braking system to malfunction and posing fall hazards to climbers.
Noble House is recalling about 3,300 dining chairs because the legs can break, posing a fall hazard. Consumers should stop using the chairs and contact the company for a free repair kit.
Chrysler is recalling 2017 Pacifica Plug-in Hybrid vehicles because the tire placard incorrectly lists seating capacity and weight limits, potentially causing vehicle overloading.
Conagra Brands is recalling approximately 717,338 pounds of spaghetti and meatball products because they contain undeclared milk, a known allergen.
Tyson Foods is recalling approximately 2.5 million pounds of ready-to-eat breaded chicken products because they may contain undeclared milk, a known allergen.
Gourmet Boutique LLC is recalling approximately 294,744 pounds of ready-to-eat breaded chicken products because they may contain undeclared milk, a known allergen.
Chrysler is recalling 2017 Pacifica Plug-In Hybrids because a power inverter defect may cause the vehicle to stop moving, increasing crash risk.
Maid-Rite Specialty Foods is recalling approximately 174,000 pounds of beef products because they contain undeclared milk, a known allergen.
Volvo is recalling 2017 XC90 vehicles because a seat belt component may detach and become a projectile, increasing injury risk.
Supreme is recalling 2007-2017 Signature Van and Kold King vehicles because rear reflex reflectors may be mounted too high, failing federal safety standards and increasing crash risk.
Cycling Sports Group is recalling about 1,000 GT mountain bicycles because the handlebars can crack, posing a fall hazard to consumers.
Porsche is recalling specific 2010-2012 Panamera and 2011 Cayenne vehicles because loose camshaft controllers may cause the engine to stall, increasing crash risk.
SCA Pharmaceuticals is recalling 70 bags of cefazolin sodium due to leaks at the seam, which compromises the product's sterility.
SCA Pharmaceuticals is recalling 30 bags of Phenylephrine HCL injectable solution because the bags are leaking at the seam, compromising sterility.
SCA Pharmaceuticals is recalling 56 bags of morphine sulfate in 0.9% Sodium Chloride injectable because the bags are leaking at the seam, compromising sterility.