State
72,820 recalls have nationwide distribution and so reach Minnesota. 7,803 additional recalls listed Minnesota specifically in their distribution scope.
Of the 7,803 recalls naming Minnesota we have scored against our rubric, 1,125 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,891 (24%) are Severe.
Which agencies issued them
These figures cover only the 7,803 recalls whose distribution notice names Minnesota specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mack Trucks is recalling 2027 Anthem and Pioneer models because center roof marker lights may fail to illuminate, reducing visibility.
OKK Trading, Inc. is recalling three models of Easter LED Headbands because the lithium coin batteries can be easily accessed by children, posing a risk of serious injury or death.
Toyota is recalling 2026 bZ Woodland vehicles equipped with a tow converter due to an electrical short circuit risk that can disable stability control and keep brake lights on.
Evenflo is recalling Revolve180 Litemax NXT child seats manufactured through March 31, 2025, because a miscalibrated level indicator may cause the seat to sit too upright, increasing injury risk in a crash.
KC Imports and Exports is recalling Laser & LED Light Mini Laser Pointer Keychains because button cell batteries can be easily accessed by children, posing a risk of serious injury or death.
Syera is recalling Space Astronaut LED Finger Lights sold on Temu because the button cell batteries can be easily accessed by children, posing a risk of serious injury or death if swallowed.
Chrysler (FCA US, LLC) is recalling certain 2023-2026 Alfa Romeo Tonale and 2023-2025 Dodge Hornet vehicles because the rear outboard seat belts may fail to retract properly.
Toyota is recalling certain 2024 Tacoma hybrid and 2024-2025 Tacoma vehicles because their rear shock absorber assemblies may corrode and fail, potentially detaching the external oil reservoir and creating a road hazard.
Chrysler is recalling specific Mopar seat belt assemblies because the rear outboard belts may twist and fail to retract, increasing injury risk.
Volvo Trucks is recalling 2026-2027 VNL and VNR models because center roof marker lights may fail to illuminate, reducing visibility.
International is recalling 2027 HV, HX, LT, MV, and RH trucks because a wiper nut may loosen, causing wipers to disconnect and reducing visibility.
ResMed is recalling Astral 100/150 ventilators because supercapacitor electrolyte leakage can damage the charger chip, trigger a fail-safe state, and interrupt ventilation therapy.
Medtronic Perfusion Systems is recalling EOPA Elongated One-Piece Arterial Cannula (Model 77522) due to potential pinhole leaks in the wire-wound body during use.
Medtronic Perfusion Systems is recalling EOPA Elongated One-Piece Arterial Cannula Model 77722 due to potential pinhole leaks in the wire-wound body during use.
Windstone Medical Packaging is recalling 15 AMS medical convenience kits containing Elevaris Lidocaine HCl injection USP due to supplier quality issues reported by Elevaris Medical Devices Inc.
Medtronic is recalling its EOPA arterial cannula because pinhole leaks may occur during bypass, risking hypovolemia, vessel injury, and organ dysfunction.
Instrumentation Laboratory is recalling the GEM Premier 5000 portable blood analyzer system because bar code reader wands may assign patient results to the wrong patient ID. The recall affects 21 units distributed nationwide.
Argon Medical Devices is recalling its L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm (REF 384620) because the hub may leak or crack, potentially causing therapy interruption, blood loss, or bloodstream infection.
Stryker GmbH is recalling Hoffmann II Carbon Connecting Rods (catalog 50796060) because they may crack after cleaning and sterilization. The recall covers all lots and about 9,658 units distributed worldwide.
Stryker is recalling Hoffmann II Carbon Connecting Rods (catalog 50796040) because they may crack after cleaning and sterilization.
Instrumentation Laboratory is recalling Bar Code Reader (BCR) wands used with GEM Premier 5000 and 7000 systems because they may assign patient results to the wrong patient ID.
Mylan Pharmaceuticals is recalling one lot of Mycophenolate Mofetil for Injection, 500 mg/vial, because precipitate was found in the vials. The recall covers 5,688 vials distributed nationwide.
Argon Medical Devices is recalling certain L-Cath PICC catheters because the hub may leak or crack, potentially causing blood loss, infection, or therapy interruption.
Medtronic recalls 21,290 EOPA arterial cannulas (BLUNT 22FR) because pinhole leaks may occur during bypass, risking hypovolemia, vessel injury, hypotension, ischemia, and organ dysfunction.
Stryker GmbH is recalling Hoffmann II Carbon Connecting Rods (catalog 50796090) because they may crack after cleaning and sterilization. The FDA classified this as a Class II recall.