State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
J. Crew is recalling specific girls' puffer coats because front buttons can detach, posing a choking hazard to young children. No injuries have been reported.
Forest River is recalling 2016 Coachmen Galleria motorhomes because the Federal Placards incorrectly list seatbelts and omit the Gross Vehicle Weight Rating, increasing crash risk.
Navistar is recalling 2016-2017 IC CE school buses because hood straps may elongate, allowing the hood to open unexpectedly during braking and obstructing the driver's vision.
Volvo is recalling 2016-2017 VNL, VNX, and VNM trucks because a missing roll pin or loose bolt may cause the steering shaft to separate, resulting in a loss of steering.
Goodman Company is expanding a recall for specific air conditioning and heating units because their power cords can overheat, posing fire and burn risks.
Mevion Medical Systems is recalling four MEVION S250 Radiation Therapy Systems because the treatment table positioning belt can slip, causing patient setup deviations.
C.R. Bard is recalling Arctic Sun 5000 and 2000 devices because a simulator key could be connected to the patient cable, resulting in improper temperature therapy.
Smith & Nephew is recalling BEAVER Blade 4.0mm orthopedic instruments because they may fracture during hip arthroscopy procedures.
Macleods Pharma USA is recalling Pramipexole Dihydrochloride tablets due to the presence of a foreign Carbimazole 5 mg tablet.
Moog is recalling specific Curlin infusion pumps because calibration errors may cause them to deliver medication faster than programmed.
DePuy Orthopaedics is recalling 351 SIGMA HP MBT Non-Keel Punch Knee Instruments due to a design defect that may cause surgical complications.
Navistar is recalling 104 model year 2016 IC CE commercial buses because hood straps may elongate, causing the hood to open unexpectedly during braking and obstructing the driver's vision.
Hain Celestial is recalling Roastaroma Herbal Tea because some packages are labeled 'Gluten Free' but contain barley.
Michaels is recalling Ashland artificial poinsettia stems and bushes because mold may be present, posing a risk of respiratory or other infections.
Biomet France SARL is recalling Endobon-Xenograft Granules because the product failed cytotoxicity tests at 36 months. Use past the 18-month shelf life may cause patient illness or injury.
Keystone is recalling 2016 Sprinter recreational vehicles because a wall-mounted television may break off, posing an injury risk to occupants.
Fagron, Inc. is recalling SyrSpend SF Grape Flavor suspending base due to the presence of yeast. The recall affects 148 bottles distributed nationwide.
Michaels is recalling Ashland holiday paper boxes because mold may be present, posing a risk of respiratory or other infections for consumers with compromised immune systems or mold allergies.
Iowa Mold Tooling is recalling certain Series III cranes because a valve bank cover may crack and fall off, creating a road hazard.
Accuray is recalling CyberKnife Robotic systems because the gun box mounting bracket may fail, allowing the gun box to fall and contact a patient.
Del Medical is recalling VS200 radiographic cassette holders and wall stands because they can suddenly fall to the ground and contact patients.
GE Medical Systems is recalling 2,111 Mavig Monitor Suspension Systems because a reported incident involved a suspension arm falling to the floor.
Del Medical, Inc. is recalling VS300 radiographic cassette holders and wall stands because the unit can suddenly fall to the bottom of its travel and contact a patient.
Zimmer Dental Inc is recalling specific dental implants because the instructions for use omitted safety information regarding the 3.7 mmD and 4.1 mmD Trabecular Metal models.
Bearded Brothers LLC is recalling BOLD The Greek energy bars due to mold. The recall covers 150 cases distributed nationwide.