State
73,806 recalls have nationwide distribution and so reach Utah. 4,916 additional recalls listed Utah specifically in their distribution scope.
Of the 4,916 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 1,351 (27%) are Severe.
Which agencies issued them
These figures cover only the 4,916 recalls whose distribution notice names Utah specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Arrow International Inc is recalling 108 units of Arrow PICC with Chloraguard Technology because the product was labeled with an incorrect expiration date.
Zydus Pharmaceuticals is recalling Pramipexole Dihydrochloride Tablets 0.25 mg due to cross-contamination caused by cleaning failures.
Arrow International Inc is recalling 1,840 units of Arrow PICC Kits because the product labels display an incorrect expiration date.
CooperSurgical is recalling 19 LEEP Precision Integrated Systems because incorrect fuses may have been installed in the generator.
Arrow International Inc. is recalling 9 units of Arrow JACC with Chloraguard Technology due to incorrect expiration dates on the product.
Zydus Pharmaceuticals USA Inc is recalling Pramipexole Dihydrochloride Tablets 0.25 mg due to cross contamination caused by a cleaning failure.
Arrow International is recalling 350 units of Arrowg+ard Blue Advance PICC catheters because the product labels display an incorrect expiration date.
Arrow International Inc is recalling 279 units of Arrowg+ard Blue Advance PICC catheters because the products display an incorrect expiration date.
Arrow International Inc is recalling 2 units of Arrow JACC with Chloraguard Technology due to an incorrect expiration date on the product label.
Sun Pharmaceutical is recalling Allergy Relief D tablets because testing showed impurities above or near specification limits.
Ecolab is recalling 183 cases of QUIK-CARE Aerosol Foam Hand Sanitizer because it was manufactured using the wrong alcohol raw material.
Arrow International Inc. is recalling 190 units of Arrow PICC Kits due to incorrect expiration dates printed on the product.
Zydus Pharmaceuticals is recalling specific lots of Methylprednisolone tablets due to cross-contamination caused by cleaning failures.
Arrow International Inc is recalling 78 units of Arrowg+ard Blue Advance JACC due to incorrect expiration dates. The recall is nationwide.
Arrow International Inc is recalling Arrowg+ard Blue Advance Midline devices due to an incorrect expiration date printed on the product.
Zydus Pharmaceuticals is recalling Methylprednisolone tablets due to cross-contamination caused by cleaning failures. The affected lots are distributed nationwide.
Zydus Pharmaceuticals is recalling specific lots of Methylprednisolone tablets due to cross-contamination caused by cleaning failures.
Zydus Pharmaceuticals is recalling specific lots of Methylprednisolone tablets due to cross-contamination caused by cleaning failures.
Arrow International Inc is recalling 450 units of Arrowg+ard Blue Advance PICC devices due to incorrect expiration dates.
Arrow International Inc. is recalling 52 units of Arrowg+ard Blue Advance JACC products due to an incorrect expiration date.
Zydus Pharmaceuticals is recalling Pramipexole Dihydrochloride Tablets 1 mg due to cross-contamination caused by a cleaning failure.
Arrow International Inc is recalling Arrowg+ard Blue Advance PICC catheters because the product has an incorrect expiration date.
Arrow International Inc is recalling 191 units of JACC central catheters because the expiration date printed on the product is incorrect.
Arrow International Inc is recalling 100 units of Arrow PICC Kits due to an incorrect expiration date printed on the product.
Sun Pharmaceutical is recalling Wal-Fex D tablets because testing showed impurity levels above or near specification limits.