State
73,363 recalls have nationwide distribution and so reach Minnesota. 7,841 additional recalls listed Minnesota specifically in their distribution scope.
Of the 7,841 recalls naming Minnesota we have scored against our rubric, 1,139 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,906 (24%) are Severe.
Which agencies issued them
These figures cover only the 7,841 recalls whose distribution notice names Minnesota specifically. The 73,363 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Toyota is recalling certain 2023 Tundra, Tundra Hybrid, and Sequoia Hybrid vehicles due to insufficiently welded spare tire carrier assemblies that may break and allow the spare tire to detach, increasing crash risk.
Newmar is recalling certain 2019–2023 motorhomes because modified seat belt mounting brackets can fail to properly restrain occupants in a crash, violating federal safety standards.
Daimler Trucks is recalling 2023-2024 Freightliner eCascadia vehicles because a defective e-axle weld may cause sudden loss of drive power, increasing crash risk.
VRURC portable chargers (model OD-B7) sold on Amazon.com from July 2021 through May 2023 can ignite and pose a fire hazard. One charger caught fire on a commercial flight, injuring four flight attendants.
woom Bikes USA recalls about 84,000 woom ORIGINAL children's bicycles from model years 2018–2021. The stem and handlebar can detach, causing riders to lose control and fall.
Yamaha is recalling about 11,000 Model Year 2023 Golf Cars, Personal Transportation Vehicles, and Umax models because the accelerator spring can become dislodged, preventing the accelerator pedal from returning to rest and posing crash, injury, and death hazards.
Husqvarna is recalling about 2,700 Residential 300 Series Snow Blowers because the auger pulley bolt can loosen, causing the drive to unexpectedly engage and potentially collide with users. No injuries have been reported.
TELEFLEX endotracheal tubes (Murphy design) may have a disconnected 15mm connector. Approximately 12,382 affected units were distributed nationwide. Healthcare facilities should inspect tubes before use.
Teleflex is recalling 18,620 endotracheal tubes due to reported disconnection of 15mm connectors. The tubes are used for oral and nasal intubation and were distributed nationwide.
Megadyne Medical Products is recalling the MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode due to reported patient burns that occurred during electrosurgical procedures.
The FDA is recalling 21,100 units of the MEGADYNE MEGA 2000 Patient Return Electrode due to reports of patient burns during electrosurgical procedures. All units distributed nationwide are affected.
Teleflex LLC is recalling approximately 10,650 units of Slick Set Uncuffed Endotracheal Tubes due to reports of 15mm connector disconnection from the tube.
TELEFLEX is recalling endotracheal tubes due to reports of 15mm connector disconnection. Approximately 25,160 units were distributed nationwide.
Teleflex is recalling 25,520 Preformed AGT endotracheal tubes due to reports of 15mm connector disconnection. This is an FDA Class I recall affecting units distributed nationwide.
Teleflex LLC is recalling 2,860 endotracheal tubes due to reports of 15mm connector disconnection. Affected tubes were distributed nationwide including Puerto Rico.
TELEFLEX is recalling RUSCHELIT Safety Clear Tracheal Tubes due to reported disconnection of the 15mm connector, affecting approximately 37,076 units distributed nationwide.
TELEFLEX is recalling 760 endotracheal tubes due to reports of 15mm connector disconnection. This medical device failure could compromise airway management during critical care.
Teleflex LLC is recalling 170,179 endotracheal tubes nationwide due to reports of 15mm connector disconnection. The tubes are used for airway management in medical facilities.
Megadyne Medical Products is recalling 21,100 units of MEGA SOFT Universal Plus Patient Return Electrodes used in electrosurgery. The FDA Class I recall follows reports of patient burns during surgical procedures.
Teleflex Slick Set endotracheal tubes (REF 170055) are being recalled by the FDA following reports of disconnection of the 15mm connector. This Class I recall affects approximately 3,530 units distributed nationwide.
Teleflex is recalling 3,309 Preformed AGT Oral Endotracheal Tubes due to reports of 15mm connector disconnection. This defect may compromise airway management during medical use.
Teleflex is recalling Slick Set Cuffed Endotracheal Tube and Stylet Sets due to reports of disconnection of the 15mm connector from the endotracheal tube. The affected units were distributed nationwide.
TELEFLEX endotracheal tubes are being recalled due to reports of the 15mm connector disconnecting from the tube. The recall affects 860,472 units distributed nationwide, including Puerto Rico.
Teleflex is recalling 37,890 Preformed AGT endotracheal tubes due to reports of 15mm connector disconnection. The devices were distributed nationwide in the United States and Puerto Rico.
Teleflex is recalling 47,520 endotracheal tubes due to reported 15mm connector disconnection. The FDA classified this as a Class I recall; disconnected tubes could compromise airway management.