State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
E-One is recalling 140 model year 2015-2016 Cyclone II, Quest II, and Typhoon emergency vehicles because pump intake strainers may be improperly soldered.
Hobby Lobby is recalling Little Wishes plush pacifier holders because parts can detach and pose a choking hazard to infants.
Hobby Lobby is recalling Little Wishes Chenille Stuffed Rattles because seams can separate, exposing stuffing and posing a choking hazard to infants.
Kovatch Mobile Equipment is recalling certain 2016-2017 emergency vehicles because pump intake strainers may be improperly soldered, potentially causing pump damage and reduced firefighting effectiveness.
Supreme Corporation is recalling 2011-2014 Signature Van, Iner-City, and Kold King vehicles because roof marker lights may short circuit and cause the corner caps to catch fire.
Back To Nature Foods is recalling Classic Creme Cookies because they contain undeclared milk. The recall covers 154,044 cartons shipped to 16 states.
B Braun Medical Inc is recalling 68 Dialog+ Hemodialysis Conductivity Sensors due to a potential leakage hazard. The units were distributed nationwide to various states and territories.
Keystone RV Company is recalling specific 2016-2017 Passport trailers because they were built with axles that have lower capacity than required, increasing the risk of axle failure and a crash.
B Braun Medical Inc is recalling 370 Dialog+ Hemodialysis machines because conductivity sensors may leak. The recall covers units distributed nationwide and in Puerto Rico.
B Braun Medical Inc is recalling 147 Dialog+ Hemodialysis Conductivity Sensors due to potential leakage. The sensors are used in dialysis machines for kidney failure patients.
Chrysler is recalling 2016 Jeep Cherokee vehicles because the left halfshaft may fracture without warning, increasing the risk of a crash.
B Braun Medical Inc is recalling 90 Dialog+ Hemodialysis machines because conductivity sensors may leak. The recall covers units distributed nationwide.
Chrysler is recalling 2016 Jeep Cherokee vehicles because the right halfshaft may fracture without warning, increasing crash risk.
B Braun Medical Inc. is recalling 40 Dialog+ Hemodialysis machines due to a potential leakage issue with conductivity sensors.
B Braun Medical Inc is recalling 318 Dialog+ Hemodialysis machines because conductivity sensors may leak. The recall covers units distributed nationwide.
Subaru is recalling 48,819 Legacy and Outback vehicles because an improperly machined steering column may cause loss of steering control, increasing crash risk.
Chrysler is recalling 2011-2016 Jeep Wranglers because dust contamination may cause the driver's air bag circuit to fail.
Ajinomoto Windsor is recalling approximately 47 million pounds of not-ready-to-eat meat and poultry products due to possible Listeria monocytogenes contamination.
Forest River is recalling specific 2016-2017 Berkshire and 2016 Cross Country recreational vehicles because front sway bar brackets may not fit properly, risking detachment and crashes.
CareFusion 303, Inc. is recalling 23,397 Alaris PC units, Model 8015, because a super capacitor failure may cause a system error code at power-up.
Applied Medical Technology Inc is recalling Wilson Penile Implantation System Retractor Frames due to a reported open pouch that breaches sterilization validation.
Great Lakes is recalling 1998-2016 Drywall Pup trailers because rear impact guards do not meet federal safety standards, increasing injury risk in crashes.
TwinGo is recalling about 4,000 baby carriers because the waist buckle can break, posing a fall hazard to children. No injuries have been reported.
Siemens is recalling eight MAGNETOM Aera/Skyra MRI systems because the patient table's docking station cover may contain a magnetic plate that attracts to the main magnet.
Applied Medical Technology Inc is recalling 1,100 units of the Wilson Implantation System after a complaint revealed an open pouch that breached sterilization validation.