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 Roasted Buffalo Broccoli served on the salad bar due to possible contamination with Listeria monocytogenes.
Whole Foods Market is recalling Salad Detox products sold nationwide from October 2019 to November 2019 due to possible Listeria monocytogenes contamination.
Medisca, Inc. is recalling specific lots of Estriol, USP (Micronized) because the product failed impurities and degradation specifications.
Whole Foods Market is recalling specific crudités vegetable platters due to possible contamination with Listeria monocytogenes.
Whole Foods Market is recalling Vegetables Stir Fry served on the hot bar due to possible contamination with Listeria monocytogenes.
Whole Foods Market is recalling Caulilini salad served on the salad bar due to possible contamination with Listeria monocytogenes.
Whole Foods Market is recalling Vegetable Korma Indian served on the hot bar due to possible contamination with Listeria monocytogenes.
Whole Foods Market is recalling Cauliflower Broccoli Romesco Basque served on the hot bar due to possible contamination with Listeria monocytogenes.
Lannett Company is recalling specific lots of Levetiracetam Oral Solution because testing found out-of-specification microbial counts.
Whole Foods Market recalled its Trend Alert Pickled Pear & Brussels Sprouts salad bar because of possible Listeria monocytogenes contamination. The product was sold nationwide from October 10, 2019 through November 4, 2019.
Whole Foods Market is recalling its Grilled Chicken & Kale Brussels Meal because possible contamination with Listeria monocytogenes was found. The nationwide recall covers products distributed from October 10, 2019 through November 4, 2019.
Whole Foods Market is recalling Chicken General Tso and Chick'n General Tso sold on the hot bar due to possible contamination with Listeria monocytogenes.
Whole Foods Market is recalling Salad Broccoli Crunch due to possible Listeria monocytogenes contamination. The product was sold nationwide from October 10 to November 4, 2019.
Whole Foods Market is recalling scalloped potatoes and broccoli served on the hot bar due to possible Listeria monocytogenes contamination.
Arrow International Inc is recalling specific Arrow Berman Angiographic Catheters due to a potential leak in the balloon extension line that could cause serious injury or death.
Whole Foods Market is recalling Chicken Cashew sold on the hot bar and in the chef's case due to possible contamination with Listeria monocytogenes.
Whole Foods Market is recalling various kale and Brussels sprouts salad products due to possible contamination with Listeria monocytogenes.
Whole Foods Market is recalling Wedge Charred Corn Salad served on the salad bar due to possible contamination with Listeria monocytogenes.
Roche Diagnostics is recalling 82 units of Homocysteine tests due to calibration failures and quality control recovery issues on cobas c 701 and 702 modules.
Whole Foods Market is recalling Salmon Dinner with Thai Curry for 2 due to possible contamination with Listeria monocytogenes.
Whole Foods Market is recalling Trend Alert Caulilini with Vadouvan Curry from salad bars due to possible Listeria monocytogenes contamination.
Angiodynamics, Inc. is recalling 60 Micro-PSD HDR sensors because they may provide readings outside the expected accuracy range.
Angiodynamics, Inc. is recalling four OARtrac PLUS Clinical Detector Units because they may produce readings outside the expected accuracy range.
Medtronic is recalling 1,297 percutaneous pin adapters because they may rotate after surgical placement and fail to return to their original position.
Carl Zeiss Meditec is recalling VisuMax software version 2.10.13 because a defect may cause a cap cut instead of a flap cut if suction is lost during treatment.