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.
Abbott Laboratories is recalling ARCHITECT Estradiol Kits because interaction with the drug Fulvestrant causes falsely elevated estradiol results.
Baxter Healthcare is recalling 6,128 COSEAL Surgical Sealant Kits because the PEG component may not fully dissolve, affecting hydrogel consistency.
Baxter Healthcare is recalling 274 units of COSEAL Surgical Sealant Kits because the PEG component may not fully dissolve, affecting hydrogel consistency.
Medscience Inc is recalling AllergiEnd ST-9 skin test applicators and trays because they were marketed without FDA clearance.
Philips Medical Systems is recalling 424 Ingenuity Core 128 CT systems because the system may not map the Varian drive after a user logout and login.
Philips is recalling 215 Ingenuity CT systems because they may fail to map the Varian drive after a user logs out and back in.
Baxter Healthcare is recalling 6,804 units of COSEAL Surgical Sealant Kits because the PEG component may not fully dissolve, affecting hydrogel consistency.
Lupin Pharmaceuticals is recalling 570 vials of Ceftriaxone for Injection USP, 2 g, because the active pharmaceutical ingredients used in manufacturing failed specifications.
Lupin Pharmaceuticals is recalling Ceftriaxone for Injection vials because they were manufactured using active pharmaceutical ingredients that failed specifications.
Lupin Pharmaceuticals is recalling Ceftriaxone for Injection USP, 500 mg, because the active ingredients used in manufacturing failed specifications.
Lupin Pharmaceuticals is recalling specific lots of Ceftriaxone for Injection USP because they were manufactured using active pharmaceutical ingredients that failed specifications.
B. Braun Medical is recalling 11,000 Non-Vented Dispensing Pins because the outer blister packaging may tear, potentially compromising the device.
Lupin Pharmaceuticals Inc. is recalling Ceftriaxone Sodium (Sterile) USP active pharmaceutical ingredient because intermediates failed specifications.
B. Braun Medical is recalling approximately 11,000 Non-Vented Dispensing Pins because the outer blister packaging may tear, potentially compromising the product label.
Thor Motor Coach is recalling 2015-2016 Tuscany motor homes because steering boxes may wear prematurely, risking sudden loss of steering.
Focus Bicycles is recalling about 80 Spine mountain bicycles because incorrectly sized seatstay or linkage parts can cause the frame to collapse, posing a fall hazard.
Daimler Trucks North America is recalling 717 Thomas Built Buses because corrosion on the emergency door handle stem could delay evacuation during an emergency.
Lakota is recalling 2016 Bighorn, Charger, and Livestock Edition trailers because pin holes in aluminum rims may cause tire failure and increase crash risk.
Meritor is recalling specific FF967 Non-Drive Front Steer axles manufactured in 2012 because they may have been incorrectly heat treated, posing a risk of fracture and loss of vehicle control.
Volkswagen is recalling specific 2016 Jetta, Passat, and Golf vehicles because the fuel rail may detach, causing a fuel leak that could lead to a vehicle fire.
Blue Bird is recalling 2015-2017 All American and 2016-2017 Vision transit buses equipped with Ricon S-Series wheelchair lifts due to potential platform cracking and bearing displacement.
Mitsubishi is recalling 2001-2002 Chrysler Sebring and Dodge Stratus vehicles with beige interiors because an incorrect part may allow the passenger sun visor to detach during airbag deployment.
Keystone RV is recalling 2016-2017 Dutchmen Kodiak recreational trailers because exposed LED light ends may short, increasing fire risk.
Spartan is recalling 2015 Gladiator and MetroStar emergency vehicles because improperly soldered pump strainers may break, potentially damaging the pump and reducing firefighting effectiveness.
Hillsdale Furniture is recalling about 20,000 children's bunk beds sold at Bob's Discount Furniture because support rails can crack or break, posing a fall hazard.