State
73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Lupin Pharmaceuticals is recalling 20 mg Lisinopril tablets because 10 mg tablets were found inside sealed 20 mg bottles.
Noven Therapeutics is recalling Daytrana (methylphenidate) transdermal systems because the delivery system failed mechanical peel and shear specifications.
Medivators is recalling Endo SmartCap Tubing kits due to a manufacturing anomaly that may cause inadequate insufflation, air bubbles, or water leaks during endoscopic procedures.
Fresenius Medical Care is recalling 2008T hemodialysis machines because they may display a false 'Remove USB Device 2' alarm when no USB device is connected.
Yusef Manufacturing is recalling 12,983 tubes of SPF 15 lip moisturizers because they contain up to 150% of the labeled amount of oxybenzone.
Degania Medical Devices is recalling specific lots of temperature sensing Foley catheters due to inadequate incoming inspection practices for the thermistor sensors.
Boston Scientific is recalling 57 units of Stretch VL Ureteral Stent Sets because they may be difficult to track over a guidewire, potentially delaying procedures.
Olympus Corporation of the Americas is recalling 265 Pleuravideoscope Model LTF-160 units because data validating compatibility with certain endo-therapy devices was missing.
Rayner Intraocular Lenses Limited is recalling RaySert PLUS RSP01 injectors due to a mismatch between the outer and inner tray expiration dates and lot numbers.
Abbott is recalling 7,347 Architect HAVAB G Reagent Kits because an erroneous concentration value was used during manufacture, resulting in a decreased amount of antigen.
Olympus is recalling 265 Pleuravideoscope units because data validating compatibility with certain endo-therapy devices was missing. Updated manuals are being provided.
Fresenius Medical Care is recalling 15,342 hemodialysis machines because a false alarm may appear when a USB device is connected.
Johnson & Johnson Vision Care is recalling specific Acuvue Oasys for Astigmatism contact lenses due to a package integrity failure found during routine testing.
Degania Medical Devices is recalling 9,137 temperature sensing Foley catheters because inadequate incoming inspection practices were used on the thermistor sensors.
Boston Scientific is recalling 40 units of Stretch VL Ureteral Stent Sets because they may be difficult to track over a guidewire, potentially delaying procedures.
Triumph is recalling 3,709 motorcycles because front brake pads may corrode and detach, increasing stopping distance and crash risk.
Jayco is recalling 2020 Jay Flight SLX travel trailers because an improperly tightened propane hose may leak, increasing the risk of fire or explosion.
Forest River is recalling 2020 StarTrans PS2 transit buses because seat belt retractors may not secure occupants properly, increasing injury risk in crashes.
Motor Coach Industries is recalling 2014-2019 J4500 and 2018-2019 J3500 motor coaches because brake hoses may crack, causing air leaks and increased stopping distances.
Blue Bird is recalling 2006-2021 Vision and 2007-2013 All American school buses because the parking brake may fail to hold the vehicle on an incline.
Blue Bird is recalling 2009-2019 Vision transit buses because the floor-mounted parking brake may fail to hold the vehicle on an incline when fully loaded.
Denso is recalling certain fuel pumps where an impeller may crack and deform. This defect can cause the engine to stall while driving, increasing the risk of a crash.
Ford is recalling specific replacement headlamps for 2013-2016 Lincoln MKZ vehicles because they may have improper beam patterns and missing markings, potentially reducing visibility.
Leviton is recalling approximately 98,000 50-ampere electrical connectors, plugs, receptacles, and inlets sold in the US and Canada due to mislabeled terminal markings that pose an electrical shock hazard.
Ducati is recalling 97 2017 Superleggera motorcycles because front brake pads may corrode and detach, increasing stopping distance and crash risk.