State
73,806 recalls have nationwide distribution and so reach Minnesota. 7,851 additional recalls listed Minnesota specifically in their distribution scope.
Of the 7,851 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 2,246 (29%) are Severe.
Which agencies issued them
These figures cover only the 7,851 recalls whose distribution notice names Minnesota specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ortho Kinematics is recalling the Vertebral Motion Analyzer (VMA) software because a bug caused errors in the Radiological Read Report.
BioMérieux Inc. is recalling 57 cartons of VITEK 2 NH ID Test Kits because they are missing desiccant, which may affect product stability.
In2Bones USA, LLC is recalling 47 CoLink Lapidus Plate XP units because right and left plates were incorrectly laser-marked.
In2Bones USA, LLC is recalling 48 units of CoLink Lapidus Plates because right and left plates were laser marked incorrectly.
Mylan Institutional, Inc. is recalling 408 cartons of Diltiazem HCl Extended-release Capsules, 120 mg, due to out-of-specification impurities.
Gourmet International Inc. is voluntarily recalling LItaly Sparkling Lemon Juice Drink because of reports of leaking caps.
Euro Diagnostica AB is recalling six lots of anti-cardiolipin ELISA kits due to an incorrect distribution label. The kits were distributed in Minnesota.
Euro Diagnostica is recalling Anti-Ro (SS-A) ELISA kits due to incorrect labeling. The label incorrectly states 'Manufactured by DiaSorin' instead of 'Distributed by DiaSorin'.
Gourmet International Inc. is voluntarily recalling LItaly Sparkling Lime Juice Drink due to packaging concerns and reports of leaking caps.
Gourmet International Inc. is voluntarily recalling L'Italy Sparkling Pomegranate Juice Beverages due to packaging concerns and reports of leaking caps.
Euro Diagnostica AB is recalling Anti-Cardiolipin ELISA kits due to incorrect labeling. The kits were incorrectly labeled as 'Manufactured by DiaSorin' instead of 'Distributed by DiaSorin.'
Gourmet International Inc. is voluntarily recalling L'Italy Sparkling Mandarin Juice Drink because of packaging concerns and reports of leaking caps.
Gourmet International Inc. is voluntarily recalling L'Italy Sparkling Grapefruit Juice Drink because of packaging concerns and reports of leaking caps.
Euro Diagnostica AB is recalling four Scl-70 ELISA kits due to incorrect distribution labeling. The kits were manufactured by DiaSorin but incorrectly labeled as manufactured by them.
Gourmet International Inc. is voluntarily recalling LItaly Sparkling Sour Cherry Juice Drink due to packaging concerns and reports of leaking caps.
MAC Trailer Mfg. is recalling 2019 Dump and Waste trailers because the wheel end nut locking device may not be properly installed, allowing the wheel end to separate from the axle.
Dexter Axle is recalling D44 trailer axles with 4,400-pound capacity because missing inner bearing races can cause hub overheating or bearing failure.
Blue Bird is recalling 2019-2020 Vision and All American school buses because certain child restraint seats may be missing a required warning label on the lower strap.
Webasto is recalling AeroVironment TurboCord and TurboDock/TurboDX charging systems because failing capacitors may cause electrical shock or fire.
Polaris is recalling about 1,300 model year 2018 RZR XP Turbo S recreational off-highway vehicles because the rollover protection structure can fracture during high-speed rollovers.
Fabform is recalling 2018 EPT dump trailers because welded hinges may fracture, causing the dump box to fall unexpectedly and increasing the risk of injury or death.
Jayco is recalling 2015-2017 Redhawk motorhomes because liquid leakage into the driver's power window switch can cause corrosion and increase the risk of a fire.
USDA FSIS issued a public health alert for Empire Kosher raw chicken products sold from September 2017 to June 2018 due to a link with a Salmonella outbreak.
Navistar is recalling 2015-2019 IC Bus school buses equipped with specific wheelchair lifts because a component may fail, allowing the platform to rise too high and increasing injury risk.
REV Recreation Group is recalling 2018-2019 Fleetwood Pulse and Holiday Rambler Prodigy motorhomes because the generator exhaust pipe may contact the waste tank, increasing fire risk.