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.
Stelpro Design is recalling about 3,600 Sonoma wall fan heaters because an internal part poses a fire hazard. Consumers should stop using the units and contact Stelpro for a free replacement.
KME is recalling 2016-2020 emergency vehicles because battery corrosion can cause electrical shorts, potentially draining the battery and preventing operation during emergencies.
Boston Scientific is recalling Imager II 5F Angiographic Catheters because the tips may detach. The recall covers 1,068,827 units distributed worldwide.
International Sprout Holding Inc. is recalling clover seed in 50 lb. bags due to possible E. Coli contamination. The product was distributed to multiple states, territories, and countries.
International Sprout Holding Inc. is recalling 13,455 lbs of clover seed due to possible E. Coli contamination. The product was distributed to multiple US states, territories, and countries.
Medtronic MiniMed is recalling 38 Paradigm insulin pumps due to cybersecurity vulnerabilities that could allow unauthorized wireless control of insulin delivery.
Whole Foods Market is recalling Green Chile Chicken Tamales because they contain undeclared milk, posing a risk to individuals with milk allergies.
Micro Therapeutics is recalling 762 Ev3 Pipeline Flex Embolization Devices because the delivery system may fracture during implantation, potentially leaving parts in the patient.
Micro Therapeutics Inc is recalling 1,050 ev3 Pipeline Flex Embolization Devices because the delivery system may fracture during implantation, potentially leaving a part in the patient.
WinCo Foods is recalling 21,264 bags of frozen Berry Medley because the product was found to be adulterated with Norovirus.
Medtronic MiniMed is recalling 23,221 Paradigm insulin pumps due to cybersecurity vulnerabilities that could allow unauthorized wireless control of insulin delivery.
Medtronic MiniMed is recalling 88,243 Paradigm insulin pumps due to cybersecurity vulnerabilities that could allow unauthorized wireless control of insulin delivery.
Medtronic MiniMed is recalling 225,498 Paradigm insulin pumps due to cybersecurity vulnerabilities that could allow unauthorized wireless control of insulin delivery.
Medtronic MiniMed is recalling 34,777 Paradigm 512 insulin pumps due to potential cybersecurity vulnerabilities that could allow unauthorized wireless control of insulin delivery.
Abbott is recalling Alinity ci-series software version 2.6.2 and earlier due to identified potential performance issues.
Medtronic MiniMed is recalling Paradigm Veo insulin pumps due to cybersecurity vulnerabilities that could allow unauthorized wireless control of insulin delivery.
Medline Industries is recalling 3,690 units of sterile 3mL syringes because voids in the packaging seal caused a loss of sterility.
Medtronic MiniMed is recalling 64,174 MiniMed Insulin Pumps (model MMT-508) due to potential cybersecurity vulnerabilities that could allow unauthorized wireless control of insulin delivery.
Medtronic MiniMed is recalling 74,496 MiniMed Paradigm Insulin pumps due to cybersecurity vulnerabilities that could allow unauthorized wireless control of insulin delivery.
RaySearch Laboratories is recalling RayStation software because virtual wedge fields may not cover the entire field, resulting in a high dose plateau.
Medtronic MiniMed is recalling 17 Paradigm insulin pumps due to cybersecurity vulnerabilities that could allow unauthorized wireless control of insulin delivery.
Carroll-Baccari, Inc. is recalling Wave Prep Tubes and single-use cups found to be contaminated with Burkholderia cepacia during an FDA inspection.
Insulet is recalling Omnipod DASH Personal Diabetes Manager devices because they may suggest inaccurate bolus amounts, potentially leading to hypoglycemia or hyperglycemia.
Bard Peripheral Vascular Inc is recalling 824 PowerPort isp MRI Implantable Ports because they may contain a tunneler with an incorrect barb tip, potentially prolonging surgical operations.
Medtronic MiniMed is recalling 30,479 Paradigm Model 511 insulin pumps due to cybersecurity vulnerabilities that could allow unauthorized wireless control of insulin delivery.