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.
McLaren is recalling 2,763 vehicles because a foam pad may corrode the fuel tank, potentially causing a leak and fire risk.
BioFinest is recalling Wintergreen Essential Oil because the packaging is not child-resistant, posing a poisoning risk to young children.
LUS Distribution Inc. is recalling approximately 2,700 hair dryers and diffusers sold in the U.S. because they lack immersion protection, posing an electrocution or shock hazard if they fall into water.
Naturo Sciences is recalling Eiji Essentials Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning to young children.
Natural Health Partners is recalling Dr. Mercola Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning to young children.
Mountain Rose Herbs is recalling specific lots of Kudzu Root because they may be contaminated with Salmonella. The product was sold nationwide in the US and in Canada.
Navistar is recalling 2019 International WorkStar and HV vehicles because insufficient axle lubrication may damage wheel bearings, potentially causing wheel separation and loss of vehicle control.
Golden State Medical Supply Inc. is recalling Losartan Potassium Tablets 25 mg because an impurity, NBMA, was detected in the active ingredient.
Aurobindo Pharma USA Inc. is recalling specific lots of Gabapentin Capsules because they were manufactured in an area with observed water leakage.
Lode-King is recalling 2015-2021 Prestige SDG53-2 step-deck semi-trailers because cargo winch mounts may fail, allowing cargo to fall off and create road hazards.
Abbott is recalling the Merlin PCS 3650 Software Upgrade Kit because a software anomaly may cause the device to use a previously programmed shock energy level without alerting the user.
Sysmex America is recalling 93 CF-70 instruments because a software mismatch may prevent the device from halting when the cover door is opened.
Diagnostica Stago is recalling STA-Deficient VIII plasma due to a risk of sample-to-sample cross-contamination that may cause falsely increased factor VIII levels.
Mercedes-Benz is recalling 2020 GLE 350 and GLE 450 vehicles because a pinched wiring harness may prevent rear side air bags from deploying correctly.
Smiths Medical ASD, Inc. is recalling Portex LineDraw Arterial Blood Sampling Syringes because the luer connectors may be broken.
Smiths Medical is recalling Portex Pro-Vent Arterial Blood Sampling Kits because some lots may have broken luer connectors.
Boston Scientific is voluntarily correcting 43 units of Nitinol Thermocouple Electrodes because they were packaged with incorrect Instructions for Use.
Aurobindo Pharma USA Inc. is recalling 2,101 bottles of Phentermine Hydrochloride 15mg capsules because they were manufactured in an area with observed water leakage.
Greiner Bio-One is recalling VACUETTE 2mL 9NC Coagulation Tubes because the sodium citrate anticoagulant levels were inconsistent. The recall affects 1,000,800 units distributed nationwide.
Life Technologies is recalling 66 units of Oncomine Dx Target Test DNA Control-IVD because the expiration date was extended prior to clearance.
Aurobindo Pharma is recalling 8,040 bottles of Levetiracetam 750 mg tablets because they were manufactured in an area with observed water leakage.
Aurobindo Pharma USA Inc. is recalling specific lots of Simvastatin 40mg tablets because they were manufactured in an area with observed water leakage.
Shanghai United Imaging Healthcare is recalling two uMI 550 PET/CT systems due to software bugs that may cause reconstruction problems and patient rescans.
B&B Pharmaceuticals is recalling Estradiol USP powder because Teflon was found in the product. The recall covers 3,825 grams distributed nationwide.
Boddingtons Plastics Ltd is recalling Endocuff Vision models ARV 110, 120, 130, and 140 to update instructions regarding contraindications and potential complications.