State
73,737 recalls have nationwide distribution and so reach Utah. 4,914 additional recalls listed Utah specifically in their distribution scope.
Of the 4,914 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 1,350 (27%) are Severe.
Which agencies issued them
These figures cover only the 4,914 recalls whose distribution notice names Utah specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
BioMed Balance is recalling Wintergreen and Sweet Birch Essential Oils because the packaging is not child-resistant, posing a poisoning risk.
Skeletal Kinetics is recalling 60 units of Ossilix MP Fil bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life.
Skeletal Kinetics is recalling Osteovation bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life, potentially increasing surgical time or causing bone formation issues.
Skeletal Kinetics is recalling SKAFFOLD CMF Impress bone void filler kits because they may not maintain setting characteristics for the labeled shelf life.
Skeletal Kinetics is recalling SKAFFOLD FLOW bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life, potentially increasing surgical time or causing incomplete bone formation.
Garland Ventures is recalling Freshness Guaranteed Five Cheese Stuffed Shells due to potential Listeria monocytogenes contamination.
Skeletal Kinetics is recalling SKAFFOLD FLOW bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life, potentially increasing surgical time or causing bone formation issues.
Skeletal Kinetics is recalling Craniosculpt bone void filler kits because they may not maintain setting characteristics for the labeled shelf life.
Akorn, Inc. is recalling Proparacaine Hydrochloride Ophthalmic Solution, 0.5%, due to chemical contamination from equipment cleaning residue.
Preferred Pharmaceuticals is recalling Lidothol Patches because the contract manufacturer misplaced or lost batch records and test results.
Shimadzu Medical Systems is recalling three Trinias DAP Meters because they were found to be outside of tolerance. The devices are used in interventional procedures.
DJO, LLC is recalling Nylatex wraps used with Intelect and V-Sonic devices because they lack appropriate latex warning labels.
Keryx Biopharmaceuticals is recalling 59,820 bottles of Auryxia (ferric citrate) tablets because they were not manufactured in conformance with the FDA-approved process.
Neocis Inc. is recalling 70 units of Gen 2 Posterior Chairside Splints due to potential mislabeling. The affected products are used in dental implantation surgery.
Neocis Inc. is recalling specific dental chairside splints because they may be mislabeled. The recall covers 70 units distributed nationwide.
Neocis Inc. is recalling 50 units of Gen 2 Anterior Chairside Splints due to potential mislabeling. The affected products are distributed nationwide.
Fresenius Kabi USA, LLC is recalling 63,067 vials of Fosaprepitant for Injection because carton labels and product inserts incorrectly state the amount of the excipient edetate disodium (EDTA).
Access Scientific LLC is recalling 1,710 Powerwand XL kits due to incorrect catheter length labels. The error may cause treatment delays or user annoyance.
Newmar is recalling specific 2016-2020 motorhomes because a damaged rear Power Distribution Module may cause exterior lights to stop working, increasing crash risk.
Autocar is recalling 82 Xpeditor vehicles from 2014-2018 because a frame cross-member may fail, causing supported components to detach and increasing crash risk.
Thor Motor Coach is recalling 2,417 motorhomes because a damaged power distribution module may cause rear lights to stop working, increasing crash risk.
Thor Motor Coach is recalling 2021 motorhomes because an improperly secured battery cable may contact the exhaust manifold and pose a fire risk. Owners should contact Thor Motor Coach for a free inspection and repair.
Altec Industries is recalling 1995-1998 A0442 aerial devices because a hydraulic cylinder end gland may fail, causing uncontrolled boom movement and increasing injury risk.
Ford is recalling 2016-2020 Lincoln vehicles because seat tilt functions may damage air bag wiring, causing unintended deployment or failure to deploy.
Ford is recalling 2020 Escape and Transit vehicles because a defective air bag component may prevent proper inflation during a crash, increasing injury risk.