State
72,969 recalls have nationwide distribution and so reach Utah. 4,902 additional recalls listed Utah specifically in their distribution scope.
Of the 4,902 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 1,091 (22%) are Severe.
Which agencies issued them
These figures cover only the 4,902 recalls whose distribution notice names Utah specifically. The 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Boston Scientific is recalling 59 TENACIO Pump with InhibiZone units, UPN 72404429, because of the potential for inflation or deflation performance issues or difficulties.
American Contract Systems is recalling gynecology, laparoscopy and hysteroscopy convenience kits that were re-gassed after a sterilization nonconformance, without validation for multiple cycles.
American Contract Systems is recalling spine, laminectomy and neuro angio convenience kits that were re-gassed after a sterilization nonconformance, without validation for multiple cycles.
American Contract Systems is recalling shoulder, hip and extremity convenience kits that were re-gassed after a sterilization nonconformance, without validation for multiple cycles.
Fisher & Paykel is recalling 51,144 Airvo 2 and myAirvo 2 humidifiers because an unintentional power disconnection may sound an audible alert for less than 120 seconds.
GE is recalling 37 LOGIQ P9 R4.5 ultrasound systems running software R4.5.7 because the Ultrasound-Guided Attenuation Parameter measurement may display inaccurate liver steatosis values.
American Contract Systems is recalling C-section convenience packs that were re-gassed after a sterilization nonconformance, without validation for multiple cycles.
Rising Pharma is recalling 2,064 bottles of Carbidopa, Levodopa and Entacapone Tablets 25/100/200 mg after a sealed bottle was found to contain the 37.5/150/200 mg strength instead.
Insulet is recalling 174,013 units of the Omnipod 5 iOS app because using the iPhone magnifier on a manual entry field while typing can duplicate a digit.
Pacific Coast Producers is recalling 1,836 cases of pear halves in pear juice, distributed by Walmart, for potential contamination with lead.
Boston Scientific is recalling 172 CXR Preconnect devices with TENACIO Pump and InhibiZone because of the potential for inflation or deflation performance issues or difficulties.
American Contract Systems is recalling radiology convenience packs that were re-gassed after a sterilization nonconformance, without validation for multiple cycles.
American Contract Systems is recalling biopsy and laparoscopy convenience kits that were re-gassed after a sterilization nonconformance, without validation for multiple cycles.
Pacific Coast Producers is recalling 609 cases of canned fruit cocktail in 100% juice for potential contamination with lead.
Now Foods is recalling 1,689 pouches of NOW Real Food Organic Unsalted Whole Raw Cashews because the product contains undeclared pine nut.
AstraZeneca is recalling 916 pre-filled syringes of Fasenra (benralizumab) Injection 30 mg/mL from one lot for lack of assurance of sterility.
Sprout Organics is recalling 9,873 cases of its Sweet Potato, Apple & Spinach baby food for potential contamination with lead.
Pacific Coast Producers is recalling 102 cases of halved pears in pear juice, distributed by Wegmans, for potential contamination with lead.
Baxter is recalling 49,200 Continu-Flo solution sets with a 4-way stopcock extension set because the IV sets may leak.
American Contract Systems is recalling labor, delivery and birthing room convenience kits that were re-gassed after a sterilization nonconformance, without validation for multiple cycles.
One Frozen is recalling 57,240 bags of Good and Gather Southwest-Style Burrito Bowl Blend because the product may contain undeclared shrimp.
Ferno-Washington is recalling 138 Ferno Power X2 powered ambulance cots because the fastening post hardware could loosen, allowing the post to detach from the cot.
Baxter is recalling 136,512 CLEARLINK System DUO-VENT solution sets across three lots because the IV sets may leak.
Diagnostica Stago is recalling 12,740 units of STA Liatest D-Di across two lots because of a potential risk of underestimating D-Dimer levels.
Boston Scientific is recalling TENACIO Pump without InhibiZone, UPN 72404420, because of the potential for inflation or deflation performance issues or difficulties.