State
73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Whole Foods Market is recalling Grilled Caulilini with Sweet Poppy Seed Sauce due to possible contamination with Listeria monocytogenes.
Teleflex Medical is recalling 526,000 Arrow EZ-IO Intraosseous Vascular Access System kits because safety caps may dislodge, risking needle stick injuries and sterility compromise.
DeRoyal Industries is recalling Warrior Recovery Knee Braces because the hinge may break, causing the brace to come apart.
Teleflex Medical is recalling 526,000 Arrow EZ-IO Intraosseous Vascular Access System kits because safety caps may dislodge, exposing needles and compromising sterility.
Whole Foods Market is recalling Family Meal Chicken Orange and Vegetable products due to possible contamination with Listeria monocytogenes.
Whole Foods Market is recalling Salmon Dinner with Mild Italian for 2 due to possible contamination with Listeria monocytogenes.
Whole Foods Market is recalling Wedge Greek Salad served on the salad bar due to possible contamination with Listeria monocytogenes.
AuroMedics Pharma LLC is recalling specific lots of Gabapentin Capsules because a Losartan/HCTZ tablet was found in the bottles.
Whole Foods Market is recalling Salmon Dinner with Lemon Herb for 2 due to possible contamination with Listeria monocytogenes.
Smith & Nephew is recalling 1,371 PROFIX Mallets because the poly tip may detach during surgery, potentially releasing particles into the surgical field.
Gold Standard Baking is recalling Freshness Guaranteed Croissants because the packaging is missing ingredient and nutrition labels, including required allergen information for milk, wheat, and soy.
Bio-Signal Group Corp. is recalling HydroDot Wave Prep single-use cups due to potential contamination with Burkholderia cepacia. The product is distributed in six US states.
Teleflex Medical is recalling 526,000 Arrow EZ-IO Intraosseous Vascular Access System kits because safety caps may dislodge, exposing needles and compromising sterility.
Whole Foods Market is recalling Caulilini, Roasted with Roasted Garlic, served on the salad bar, due to possible contamination with Listeria monocytogenes.
Bio-Signal Group Corp. is recalling HydroDot Wave Prep electroconductive cream due to potential contamination with Burkholderia cepacia.
Polymer Technology Systems is recalling A1CNow+ Systems because a software bug may display incorrect numerical values instead of expected symbols.
Polymer Technology Systems is recalling ReliOn FastA1C Tests due to a software bug that may display incorrect numerical values instead of expected symbols.
Lupin Pharmaceuticals is recalling 3,726 bottles of Memantine Hydrochloride Extended-release Capsules because stability studies showed high out-of-specification dissolution results.
Angiodynamics, Inc. is recalling 160 OARTRAC Prostate Immobilization Endorectal Balloon Device Kits because they may produce readings outside the expected accuracy range.
Angiodynamics, Inc. is recalling 36 units of MICRO-PSD Electron sensors because they may provide readings outside the expected accuracy range.
Polymer Technology Systems is recalling 15,118 Walgreens At-Home A1C Test Kits due to a software bug that may display incorrect numerical values for extreme results.
Polymer Technology Systems is recalling CVS Health At Home A1C Test Kits due to a software bug that may display incorrect numerical values for extreme results.
Teleflex Medical is recalling Sheridan Endobronchial Tubes due to incorrectly labeled tracheal and bronchial swivel connectors.
Integra Lifesciences is recalling nine Ascension Silicone PIP implants that were mislabeled as size 1 but contained size 0 implants.
Angiodynamics, Inc. is recalling 48 Micro-PSD External Beam Photon sensors due to potential accuracy issues. The devices are used to measure radiation therapy during cancer treatment.