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.
BMW is recalling specific 2014-2016 MINI and i3 vehicles because the passenger air bag may not deploy properly in a low-speed crash, increasing injury risk.
Hyundai is recalling 28,157 model year 2011 Elantra and Sonata vehicles because road salt may corrode front coil springs, potentially causing them to fracture and puncture tires.
Arrow International Inc. is recalling Arrow Kits containing Medtronic Covidien 0.9% Sodium Chloride Flush Syringes due to compromised sterility of the outer barrel.
MicroPort Orthopedics is recalling Profemur Plus modular neck hip prosthesis components due to an unexpected rate of postoperative fractures requiring revision surgery.
Volkswagen is recalling 993 model year 2015 Jetta, Golf, and E-Golf vehicles because the passenger air bag may not deploy properly in a crash.
Medistat RX L.L.C. is recalling all sterile products, including various injectable medications, due to a lack of assurance of sterility.
General Mills is recalling specific lots of Cascadian Farm Organic Cut Green Beans because one package tested positive for Listeria monocytogenes.
Biosense Webster is recalling SOUNDSTAR eco 8F and 10F Diagnostic Ultrasound Catheters because the ultrasound image may disappear if the CARTO 3 system restarts during a pericardial effusion.
Medtronic Navigation is recalling 2,346 Navigated Solera Screwdrivers used in spine surgery because specific use conditions may cause the tips to deform or break.
Biosense Webster is recalling the Carto 3 EP Navigation System because the ultrasound image may disappear during use, requiring a system restart.
Volvo is recalling 2015-2016 VAH and VHD trucks because some headlights do not meet federal intensity requirements, increasing crash risk.
Nutraceutical International is recalling KAL Amino Acid Complex because the ingredient list does not explicitly state 'milk,' despite containing casein.
BRP is recalling about 240 Youth Model Can-Am DS 90 and DS 90X ATVs because a fuel filter defect can cause leaks and fire. No injuries have been reported.
Medtronic Navigation is recalling 2,346 Solera screwdrivers used in spine surgery because specific conditions may cause the tips to deform or break.
MicroAire Surgical Instruments is recalling 168 LipoTower units due to a risk of electrical shock if internal lead wires detach and the ground connection fails.
Ferno-Washington Inc is recalling 72 Ferno iNX Wheeled Stretchers because hole elongation in the load frame may allow the retention pin to move.
MicroAire Surgical Instruments is recalling three LipoTower units with aspiration pumps due to a potential risk of electrical shock if internal lead wires detach.
Zimmer, Inc. is recalling 112,568 sterile guide wires because the labels state a 10-year expiration date, while testing supports only 5 years.
Lifeline Systems is recalling 8,616 Philips GoSafe Mobile Help Button devices because irregular battery disconnection can cause charging issues.
Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution compact foundation because the salicylic acid ingredient is subpotent.
Sterilmed is recalling 43 reprocessed Zimmer tourniquet cuffs because they are labeled as single hose but are actually dual hose devices.
Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution Compact Foundation because the salicylic acid ingredient is subpotent.
Olympus is recalling 1,014 EVIS EXERA II Gastrovideoscopes because specific cleaning accessories required for reprocessing were not provided.
Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution Compact Foundation because the salicylic acid ingredient is subpotent.
Guthy-Renker LLC is recalling specific lots of Rodan & Fields Proactiv Solution Compact Foundation because the salicylic acid ingredient is subpotent.