State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
SureFit is recalling about 900 riding lawn mower blade spindle shafts and assemblies because they can break and become projectiles, posing an impact injury risk.
Sterilmed Inc is recalling 112 reprocessed St. Jude Medical Agilis NxT Steerable Introducers due to inadequate seals caused by missing adhesive glue.
Forest River is recalling 2018 Glaval Legacy buses because improperly tightened brake caliper bolts may cause the calipers to detach, reducing braking power and increasing crash risk.
L3 Security & Detection is recalling 471 Examiner 3DX 6000 cabinet X-ray systems used for airline baggage screening due to shielding gaps that may cause excessive X-ray emissions.
Philips is recalling specific IntelliVue patient monitors and measurement servers because they may display distorted ST-segments during 12-lead ECG monitoring.
Medline Industries is recalling 5,722 units of sterile elastic bandages because they may not have been properly sterilized.
Remel Inc is recalling Shigella sonnei Agglutinating Serum because it may fail to agglutinate within the specified minimum reaction time.
Pharmedium Services LLC is recalling morphine sulfate injection due to incorrect or missing lot and expiration dates on the labels.
Pharmedium Services LLC is recalling Hydromorphone HCl Injection due to incorrect or missing lot and expiration dates.
Pharmedium Services LLC is recalling specific lots of compounded morphine sulfate injection because the labels may have incorrect or missing lot and expiration dates.
Keryx Biopharmaceuticals is recalling Auryxia (ferric citrate) tablets because damaged silica gel packets may allow desiccant granules to contact the medication.
Takata is recalling specific 2009 model year air bag inflators that may explode due to propellant degradation. This affects vehicles registered in 22 specific states.
Takata is recalling specific frontal passenger air bag inflators in 2010 vehicles registered in 22 states and D.C. due to a risk of explosion causing serious injury or death.
Forest River is recalling 2018 Surveyor recreational trailers because an incorrect circuit breaker can cause wiring to melt, increasing the risk of a fire.
Takata is recalling specific 2013 model year air bag inflators in 13 states and territories due to a risk of explosion from propellant degradation.
Comfort Research is recalling about 1,200 Ultra Lounge bean bag chair covers due to risks of entrapment and suffocation to children.
Erwin Hymer is recalling 2012-2018 motorhomes because the installed fire extinguishers may clog and fail to discharge properly.
ShowHauler is recalling 2003-2018 Garage Coach, Toter Coach, and Motorhome vehicles because their fire extinguishers may clog or detach, posing injury risks during a fire.
Volvo is recalling 2016-2018 9700 buses because loose hardware on the power supply cable may cause the fuse box to overheat, increasing fire risk.
Forest River is recalling 2017-2018 Georgetown recreational vehicles because missing plugs in the brake system may cause fluid leaks or air ingestion, increasing stopping distance.
Land of Nod is recalling Nook toddler beds because the headboard can disconnect and fall, posing an entrapment risk to children.
Western Gas is recalling under-odorized propane gas due to fire, explosion, and burn hazards. Consumers should contact their supplier for a free inspection.
Old Dutch Foods is recalling Lund's & Byerly's Chipotle Ranch Potato Chips because a seasoning ingredient contains milk that may be contaminated with Salmonella.
EZWeightLossTX LLC is recalling LaBri's Body Health XPLODE capsules because they contain sibutramine, an unapproved drug ingredient.
Advanced Pharma Inc. is recalling Nitroglycerin injection syringes found to be subpotent, meaning they contain less active ingredient than labeled.