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.
Horizon Hobby is recalling E-flite Ultra Micro-4 AC/DC Battery Chargers because they can overheat and cause fires. No injuries have been reported.
BMW is recalling 2002-2005 MINI Cooper and Cooper S vehicles because the power steering system may fail, requiring extra effort to steer and increasing crash risk.
DePuy Orthopaedics is voluntarily recalling select lots of the Specialist 2 Intramedullary Rod 400mm Instrument because the rod has fractured, leaving portions inside patients.
Newmar is recalling 119 model year 2007-2008 motorhomes because tight wheel bearings may overheat and cause a fire.
Mercedes-Benz is recalling 2014-2016 S63 AMG vehicles because a software error may cause the engine to stall and fail to restart, increasing crash risk.
The RV Factory is recalling 2015-2016 Avion Azure motorhomes because an improperly placed weld on the underfloor seat bracket may cause the bracket to break in a crash, increasing injury risk.
Beckman Coulter is recalling MICroSTREP plus 1 and 2 panels because a manufacturing error may cause antimicrobial degradation and false resistant results.
Olympus is recalling MAJ-1606 Instrument Channel Adaptors due to small puncture marks in sterile packaging that may compromise sterility.
General Mills is recalling a limited quantity of frozen Cascadian Farm Cut Green Beans after one package tested positive for Listeria monocytogenes.
Toyota is recalling 2016 Tacoma trucks because incorrect bolts were used to install the driver's knee air bag module, which may loosen over time.
TCC Cooking Company is recalling CHEFS vertical roasters because they can break or shatter, posing burn and laceration hazards. No injuries have been reported.
Mercedes-Benz is recalling 2,618 model year 2014-2015 B-Class Electric Drive vehicles because a communication error may cause the electric powertrain to shut down, temporarily immobilizing the vehicle.
Caribou Coffee Company is recalling Almond Biscotti because soy lecithin was missing from the ingredient list.
Caribou Coffee Company Inc. is recalling two types of biscotti because soy lecithin was missing from the ingredient list.
Siemens Medical Solutions USA is recalling 21 SOMATOM Force computed tomography systems due to software and firmware bugs.
Mercedes-Benz is recalling 2,580 model year 2015 S550 4Matic, AMG S63, and AMG S65 vehicles because front seat belts may be installed on the wrong side, affecting crash protection.
CooperSurgical is recalling LEEP REDIKIT surgical kits because the labels list 2% Lidocaine HCl, but the kits contain 1% Lidocaine HCl vials.
Medtronic is recalling 777 identification cards for SureScan pacemaker patients that incorrectly indicate the entire system is MR Conditional.
Siemens Medical Solutions USA is recalling 113 SOMATOM Definition Flash CT scanners due to a software bug in version VA48A_SP0 that affects visual warnings and image quality.
Siemens Medical Solutions is recalling 113 SOMATOM Definition AS CT scanners to fix a software bug affecting visual warnings and image quality.
GE Healthcare is recalling 921 Centricity PACS IW systems worldwide because images may be missing when a specific system parameter is set to a value greater than 1.
Beckman Coulter is recalling MICroSTREP plus 1 and 2 panels because a manufacturing error may cause antimicrobial degradation, leading to false resistant results.
Beckman Coulter is recalling Access Free T3 Reagent Kits because they were filled incorrectly and contain insufficient reagents.
Siemens Medical Solutions is recalling 113 SOMATOM Definition Edge CT scanners due to a software bug affecting visual warnings and image quality.
Noven Pharmaceuticals is recalling Daytrana (methylphenidate) 30 mg patches due to a defective delivery system that failed mechanical peel force specifications.