State
73,718 recalls have nationwide distribution and so reach Minnesota. 7,849 additional recalls listed Minnesota specifically in their distribution scope.
Of the 7,849 recalls naming Minnesota we have scored against our rubric, 1,137 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,245 (29%) are Severe.
Which agencies issued them
These figures cover only the 7,849 recalls whose distribution notice names Minnesota specifically. The 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Blue Bird is recalling 96 2022 Vision and All American transit buses because a check valve defect may cause unintended spring brake application, increasing crash risk.
Kawasaki is recalling about 70 2021 BRUTE FORCE 750 ATVs because loose fuel pump bolts can cause fuel leaks and fire. No injuries have been reported.
Kawasaki is recalling about 100 2021 Teryx off-highway utility vehicles because loose fuel pump bolts can cause fuel leaks and fire. No injuries have been reported.
HME is recalling 2013-2021 AF1, 1871, and SFO vehicles because cracked wiring insulation may cause aerial controls to fail, creating a shock risk.
Navistar is recalling certain 2019-2021 International LT and RH trucks due to wrist pin cracks that can cause connecting rod failure and engine stalls. Affected owners should contact their dealer for free repair.
Chrysler is recalling 2020-2021 Dodge Durango vehicles because the side curtain air bag fastener may be loose or missing. A loose fastener could cause incorrect air bag deployment, increasing injury risk.
Dennis Eagle is recalling 2017-2021 Elite and Proview vehicles because documents may list the wrong weight rating, potentially leading to overloading and crashes.
YYBA is recalling Welmate Lidocaine Numbing Cream because the packaging is not child-resistant, posing a risk of poisoning to young children.
Nissan is recalling 2021 Rogue vehicles because the rear brake calipers may be missing an internal bushing, causing brake fluid to leak and reducing braking performance, increasing the risk of a crash.
HME is recalling 2016-2021 AF1 and 1871 vehicles because the self-leveling function may malfunction, causing the aerial bucket to move unexpectedly and increasing injury risk.
Dennis Eagle is recalling 2017-2021 Elite and Proview vehicles because the hard copy owner's manual was not supplied, which may lead to improper operation.
Spartan Chemical is recalling 19,044 containers of Lite'n Foamy Lemon Blossom Hand Sanitizer because a lot tested positive for Burkholderia multivorans.
Novo Nordisk is recalling Levemir FlexTouch insulin pens stored below 32°F, which may cause lack of efficacy and damage to the cartridge and pen-injectors.
Novo Nordisk is recalling Fiasp insulin cartridges stored below 32°F, which may cause lack of efficacy and damage to the cartridge and pen-injectors.
Spartan Chemical Co Inc is recalling 400 gallons of Antiseptic Hand Cleaner due to CGMP deviations. The product was distributed nationwide in the US, Puerto Rico, and Mexico.
Novo Nordisk is recalling Fiasp insulin pen samples stored below 32°F. The temperature abuse may cause lack of efficacy and damage to the cartridge and pen-injectors.
Bentley is recalling 2021 Bentayga vehicles because a rear axle lock nut may break due to stress corrosion, potentially causing loss of control.
Novo Nordisk is recalling Xultophy 100/3.6 samples stored below 32°F. The temperature abuse may cause lack of efficacy and damage to the cartridge and pen-injectors.
Novo Nordisk is recalling TRESIBA (insulin degludec) samples stored below 32°F, which may cause lack of efficacy and damage to the cartridge and pen-injectors.
Novo Nordisk is recalling Fiasp (insulin aspart injection) samples stored below 32°F, which may cause lack of efficacy and damage to the cartridge and pen-injectors.
Novo Nordisk is recalling specific lots of TRESIBA insulin pens because they were stored below 32°F, which may reduce efficacy and damage the device.
FDA recalls 11,391 units of Covidien Signia vascular stapler reloads because a safety interlock may fail, allowing empty reloads to fire and cause tissue injury.
Roche is recalling the cobas Liat Analyzer respiratory virus panel due to invalid or false positive results for SARS-CoV-2 and Influenza A/B.
Vermeer is recalling 2015-2021 AX19 brush chipper trailers because a crack in the undercarriage frame may cause it to bend, increasing the risk of a crash.
FDA is recalling specific lots of Covidien Signia stapler reloads because a safety interlock may fail, allowing empty reloads to be fired and causing tissue injury.