State
73,096 recalls have nationwide distribution and so reach Minnesota. 7,838 additional recalls listed Minnesota specifically in their distribution scope.
Of the 7,838 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 1,904 (24%) are Severe.
Which agencies issued them
These figures cover only the 7,838 recalls whose distribution notice names Minnesota specifically. The 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Hyundai is recalling certain 2025 IONIQ 5 "N" vehicles with left-foot braking because a software defect in the electronic brake and vehicle control systems may reduce braking performance, increasing crash risk.
Thy Trading Company recalls approximately 720 roll-up window blinds sold on Wayfair.com due to long operating cords that pose strangulation and entanglement hazards to children. Consumers should stop using the blinds immediately and request a full refund.
Pella Corporation is recalling about 340 Pella Reserve and Lifestyle sliding patio doors and windows because their sensor panels and remote controls contain button cell batteries that children can easily access, posing an ingestion hazard.
UVIPC Baby Gates sold on Amazon have been recalled due to an entrapment hazard that violates federal safety regulations, as children's torsos can fit through gaps in the gate design. No injuries have been reported.
TravisMathew recalled approximately 59,450 women's and men's hoodies and sweatshirts sold from January through October 2024 due to violation of federal flammability standards, posing a burn hazard.
Doosan Bobcat is recalling about 552 AirFX Finish Mower Deck attachments because the locking pins may fail to secure the deck during maintenance, creating a crush hazard. No injuries have been reported.
Ariens snow throwers may continue rotating after the operator releases the control lever, creating a laceration hazard. The company is offering free repairs at authorized dealers.
About 18,650 sling carriers sold on Temu.com violate federal safety regulations for structural integrity and occupant retention, posing a fall hazard to babies. No injuries have been reported.
Zeekr is recalling one 2025 RT vehicle because the tire pressure warning light may not flash long enough for drivers to notice.
Firefly Integrations is recalling specific G12 Electronic Control Modules installed in Thor Motor Coach vehicles due to a software error that may allow the awning to extend while driving.
Hyundai is recalling certain 2025 Ioniq 5 electric vehicles because the rear floor wiring harness may contain an open circuit, preventing the rear side air bag from deploying as intended and increasing injury risk in a crash.
General Motors is recalling certain 2022 GMC Sierra 1500 vehicles with chrome front grille deflectors because attachment points may fracture, causing the grille to detach and become a road hazard.
Toyota is recalling certain 2024–2025 Tacoma 4-wheel drive vehicles because rear brake hoses can be damaged by mud and dirt buildup, causing brake fluid leaks that reduce braking ability and increase crash risk.
Toyota is recalling certain 2025 Lexus NX and other vehicles because the second-row center seat belt webbing may be damaged, potentially reducing occupant restraint in a crash.
Astellas Pharma recalls Prograf (tacrolimus) 0.5 mg capsules distributed nationwide due to empty capsules in bottles. Affected lot 0E3353D expires March 31, 2026.
Corfu and Mediterranean brand tzatziki sauce in half-gallon tubs and 5-gallon pails are being recalled for potential Salmonella contamination. Consumers should not eat the affected products.
Samsung SDI is recalling high-voltage battery packs installed in Chrysler, Volkswagen/Audi, and Ford vehicles because they may fail, increasing the risk of a crash or fire.
Medline Industries is recalling 942 arterial line insertion kits due to excess material on the catheter hub of the catheter subassembly. The manufacturing defect prompted a FDA Class I recall of products distributed nationwide.
The Mochi Ice Cream Company is recalling My Mochi Sorbet Peach Mango Sorbet nationwide due to undeclared egg allergen. Consumers with egg allergies should not consume this product.
Astellas Pharma is recalling Astagraf XL (tacrolimus) due to manufacturing defects; bottles shipped nationwide may contain empty capsules instead of medication.
Medline arterial line tray kits (models ART600 and ART690) are being recalled because the catheter hub contains excess material from manufacturing. The recall affects 58 kits distributed nationwide.
The FDA is recalling approximately 33,589 BD Pyxis MedStation automated dispensing cabinets due to door latch assembly failures that may leave doors open, potentially delaying medication access and enabling medication diversion.
Boston Scientific is recalling HOT AXIOS Stent systems due to potential outer sheath detachment that can prevent proper stent expansion. This defect may require device replacement during the procedure.
LivaNova is recalling approximately 8,223 SenTiva VNS Therapy generators due to a potential internal component failure that may cause the implanted device to stop delivering seizure therapy. Affected patients should contact their physician.
McKesson is recalling Inflectra (infliximab-dyyb) injectable drug due to manufacturing quality deviations. A batch intended for quarantine was inadvertently distributed to patients nationwide.