State
72,984 recalls have nationwide distribution and so reach Minnesota. 7,805 additional recalls listed Minnesota specifically in their distribution scope.
Of the 7,805 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 1,892 (24%) are Severe.
Which agencies issued them
These figures cover only the 7,805 recalls whose distribution notice names Minnesota specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
eL18-4 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
L11-3 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
S7-3t Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
X3-1 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
The C10-3v Transducer Probe is the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
XL14-3 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
L10-4LAP Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
C5-2 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
S4-1 Lumify Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
C9-5ec Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
X8-2t Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
mC12-3 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
D5cwc Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
The L15-7IO Transducer Probe is the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
S12-4 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
HoMedics Air Compression Leg Massagers, model SR-160HJ, are recalled for a regulatory documentation error and a misleading color packaging claim. The record states the affected lots do not present a risk of harm.
3D6-2 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
PACCAR is recalling Kenworth T680, T880, and W990 trucks from 2024–2026 because the 15-inch digital display may fail to show warning lights or vehicle speed, increasing crash risk.
Mazda is recalling certain 2025 Mazda CX-90 vehicles (also 2024 CX-90 and 2025 CX-70 mild hybrid models) because the fuel gauge may display an inaccurate reading, which could cause unexpected stalling and increase crash risk.
Altec is recalling certain 2011-2025 Aerial Device, Digger Derrick and Service Body vehicles because the cable step wire rope assembly may be improperly secured, allowing the entry step to detach.
New Flyer is recalling specific electric bus models because an inadequate weld and software error may cause battery modules to overheat, increasing the risk of fire.
Motor Coach Industries is recalling specific 2020-2025 electric buses because an inadequate weld and software error may cause battery overheating and fire.
Kibbi is recalling 2024-2025 Renegade Verona and Verona LE recreational vehicles because a rear bracket may deflate the air suspension, increasing crash risk.
Fontaine Trailer Company is recalling 2025-2026 forklift trailers because misinstalled cables may disable the anti-lock brake system, increasing crash risk.
Tuff Trailer USA is recalling 2024 TTA17200T and TTA18200T trailers because incorrect GVWR labels may lead to overloading and coupler failure.