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.
Arrow International is recalling 416,055 Pressure Injectable Multi-Lumen Central Venous Catheterization Kits because unsealed packaging may compromise product sterility.
BMW is recalling 2018-2019 X3 vehicles because the steering wheel may fail to detect if the driver's hands are off the wheel, increasing crash risk.
Ohio Hickory Harvest is recalling Liberty Snacks Honey Roasted Cashews due to Listeria monocytogenes found in a product stored in the same bin.
Arrow International Inc is recalling 8Fr Catheter Clamps with Fasteners because unsealed packaging may compromise product sterility.
Ethicon Endo-Surgery Inc is recalling HARMONIC ACE Shears because an internal component may cause continuous or inadvertent activation of the device.
Roche Molecular Systems is recalling 163 MagNA Pure 24 automated clinical sample extractors due to reported cross-contamination of samples during rack-based purification runs.
Arrow International Inc is recalling Pressure Injectable ARROWg+ard Blue PLUS(R) Two-Lumen Central Venous Catheterization Kits because unsealed packaging may compromise product sterility.
Arrow International is recalling Arterial Line Kits because unsealed packaging may compromise product sterility. The recall covers 416,055 units distributed in the US and 33 other countries.
Arrow International is recalling 416,055 Arterial Catheterization Kits because unsealed packaging may compromise product sterility.
Respire Medical is recalling the Pink H/S Oral Sleep Apnea Device because it may break during use.
Arrow International is recalling 416,055 PSI kits because unsealed packaging may have compromised sterility. The recall covers products distributed in the US and 34 other countries.
Medline is recalling Sterile Needle Counters because packaging seal creep may compromise sterility. The recall covers 38,464 units distributed in the US, Canada, and other countries.
Arrow International is recalling 416,055 continuous nerve block needles because unsealed packaging may compromise product sterility.
Arrow International is recalling 416,055 units of Peel Away Sheath over Dilator because unsealed packaging may compromise product sterility.
Medline Industries Inc is recalling MEDLINE O.R. Necessities Sterile Needle Counters because packaging seal creep may compromise sterility.
Arrow International is recalling 416,055 central venous catheter kits because unsealed packaging may compromise product sterility.
Respire Medical is recalling 29 units of the Pink+ Hard/Soft Oral Sleep Apnea Device due to a potential for device breakage during use.
Arrow International Inc is recalling 416,055 PICC sets because unsealed packaging may have compromised product sterility.
Arrow International Inc is recalling 416,055 units of 9 Fr. Radiopaque Polyurethane Sheath/Dilator because unsealed packaging may compromise product sterility.
Arrow International Inc is recalling 416,055 ARROWgard Blue PLUS Multi-Lumen CVC Kits because unsealed packaging may compromise product sterility.
Arrow International is recalling specific lots of ARROWg+ard Blue PLUS catheterization kits because unsealed packaging may compromise product sterility.
Respire Medical is recalling the Respire Pink H/S Oral Sleep Apnea Device due to a potential for device breakage during use.
Arrow International is recalling 416,055 Maximal Barrier Drapes because unsealed packaging may compromise product sterility. The recall covers lots distributed in the US and 34 other countries.
Arrow International is recalling 416,055 central venous catheterization kits because unsealed packaging may compromise product sterility.
Genesee BioMedical is recalling 444 Sternal Valve Retractors used in cardiac surgery due to corrosion that may cause the bearing or button to break.