State
72,992 recalls have nationwide distribution and so reach Utah. 4,902 additional recalls listed Utah specifically in their distribution scope.
Of the 4,902 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 1,091 (22%) are Severe.
Which agencies issued them
These figures cover only the 4,902 recalls whose distribution notice names Utah specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Stryker Spine is recalling the Monterey AL Implant Inserter because the gold unlock button may separate from the device, which could affect functionality during surgical procedures.
Stryker Corporation is recalling Nasopore nasal dressings due to defects in blister seals that may compromise sterility. Affected products may have bubbles on the seal, indicating the sterile barrier has been breached.
BD Connecta Luer-Lok 360 stopcocks were distributed with non-U.S. instructions for use. Healthcare facilities should verify they have the correct U.S. instructions before using affected lot numbers.
Stryker Corporation is recalling 182,344 Otopore Cylinder Standard outer ear dressings due to potential defects in blister seals that may compromise sterility. Bubbles in packaging seals indicate the sterile barrier is breached.
Volkswagen is recalling certain 2025 Audi Q6 e-tron and SQ6 e-tron vehicles because the rearview camera may show a blurry image, failing FMVSS 111.
Reichert is recalling 1,876 units of the Phoroptor VRx Digital Refraction System (Model 16242) due to an assembly defect that could cause the refraction head to detach during eye examinations.
Ethicon Endo Surgery recalls ETHIBOND EXCEL surgical sutures worldwide due to curing issues with the silicone coating on the needles identified during manufacturing.
Stryker Corporation is recalling Nasopore nasal dressings due to potential breaches in packaging sterility seals that could compromise product sterilization. Approximately 182,344 units have been distributed nationwide.
Nestle-USA recalls Lean Cuisine Butternut Squash Ravioli for potential wood-like foreign material. Approximately 50,611 cases distributed across 36 states are affected.
Chicco is recalling specific MyFit Zip Air Harness and Booster child seats because they may allow excessive chest movement in a crash, increasing injury risk.
Stryker is recalling Nasopore Standard 4cm nasal dressings because the blister seals may develop bubbles, potentially compromising the sterility barrier. Affected units should not be used.
Stryker Corporation is recalling Otopore Square outer ear wound dressings nationwide because sterile packaging seals may develop bubbles, indicating a potential breach of the sterile barrier. Consumers should stop using affected units and contact their healthcare provider.
Stryker Spine has recalled 56 units of the Monterey AL Implant Inserter due to potential separation of the gold unlock button. This could impair the device's function during surgical implant placement.
Stryker Corporation is recalling 182,344 units of Hemopore nasal/sinus wound dressing due to potential packaging seal defects that could compromise sterility. A bubble on the blister seal may indicate the sterile barrier has been breached.
Good & Gather baby vegetable puree (4 oz) is being recalled due to elevated levels of lead. The recall affects 25,600 units distributed nationwide by Target.
Stryker Corporation is recalling 182,344 units of Hemopore 2PK nasal/sinus wound dressing due to potential bubbles in blister seals that indicate sterility breach. Affected lot numbers are 2024020221, 2024051720, and 2024082321.
Amerisource Health Services is recalling Voriconazole 50 mg tablets distributed nationwide due to current Good Manufacturing Practice deviations related to repackaging.
Glenmark Pharmaceuticals is recalling Chlorpromazine Hydrochloride Tablets due to a manufacturing quality deviation involving an impurity above recommended limits.
Ethicon Endo Surgery recalls PDS PLUS VIO surgical sutures with needles due to silicone curing defects during manufacturing. 792 units were distributed worldwide.
Alliance RV is recalling certain 2025 Avenue 23ML travel trailers because the Federal Placard may show incorrect unloaded vehicle weight and cargo carrying capacity.
Tolterodine Tartrate Extended-Release Capsules, 2 mg (Lot T05393) are being recalled because they failed dissolution specifications. The capsules may not dissolve as intended.
Micro Bird is recalling 2023 G5 transit buses because u-bolts securing the suspension may break, increasing crash risk.
White River Marine Group is recalling 2024-2025 Trailstar TRL and Topper boat trailers because the winch strap may fray and break, allowing the boat to detach.
Micro Bird is recalling 2023-2024 G5 school buses because u-bolts securing the suspension may break, increasing crash risk.
ILJIN Hysolus is recalling specific CNG tanks because the pressure relief device may not fully vent, potentially causing the tank to rupture and increasing the risk of fire and injury.