State
72,933 recalls have nationwide distribution and so reach Minnesota. 7,804 additional recalls listed Minnesota specifically in their distribution scope.
Of the 7,804 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 7,804 recalls whose distribution notice names Minnesota specifically. The 72,933 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Chrysler is recalling specific Mopar side curtain air bags because improperly sealed seams may cause insufficient pressure retention, increasing the risk of ejection and injury during a crash.
Sunnyyes LED mini lights are being recalled because the lithium coin batteries can be easily accessed by children, the remote battery compartment screw does not stay attached, and the packaging lacks required warnings.
Chrysler is recalling certain 2022–2026 Voyager and Pacifica vehicles because the right and left side curtain airbags may have insufficient pressure retention due to improperly sealed seams, increasing the risk of ejection and injury during a crash.
ABC Bus is recalling specific Van Hool bus models because the front entrance door window may have incorrect glazing, which could reduce driver visibility and increase crash risk.
Gillig is recalling 2023-2024 Low Floor transit buses because the rear weight placard may exceed tire ratings, increasing crash risk.
AirClub convertible bassinets are being recalled because the mechanism used to attach the product to an adult bed creates an opening between the bedside sleeper and the mattress, posing a fall hazard to infants.
GLMZZ Fidget Magnet Ball Toy Sets are being recalled because they are high-powered magnets, violating the mandatory standard for toys and posing an ingestion hazard to children.
CCCEI power strips are being recalled because they do not contain supplementary overcurrent protection, creating a fire risk if overloaded. Two reports of sparking and melting have been received.
Petzl America is recalling Nomic and Ergonomic ice climbing axes because the shaft can break at the handle during use. Twenty-six shaft breakages have been reported, with no injuries.
MPINOI adult portable bed rails are being recalled because users can become entrapped within the rail or between the rail and mattress, and the rails lack the required hazard warning labels.
Plunge Buddy is recalling DIY Sauna Heater Kits because electrical conductors within the kits can overheat. Twelve reports of overheating have been received, with no fires or injuries.
DuraTrac is recalling stainless steel gas connectors sold between May and November 2025 because a manufacturing defect could cause a gas leak, posing a fire hazard.
Cardinal Health is recalling Webcol Alcohol Prep pads because of non-sterility, with microbial contamination identified as Paenibacillus phoenicis. The FDA has classified this recall as Class I.
Volvo Trucks is recalling certain 2025-2026 VNL (4) vehicles because the service brake may take longer than expected to release, creating a crash risk and violating Federal Motor Vehicle Safety Standard 121.
Nissan is recalling 2026 Leaf vehicles because internal damage in the high voltage battery may cause a short circuit, increasing the risk of a fire.
USDA FSIS issued a public health alert for raw Blackwing organic beef and pork products produced without federal inspection. Consumers are urged to discard or return these items.
Volvo Trucks is recalling certain 2025–2026 VNL (4) vehicles because the instrument panel may fail while driving, potentially hiding critical safety information like the speedometer and warning lights.
Howmedica Osteonics is recalling the MICS3 Angled Sagittal Saw Attachment because the external screws securing the cover to the saw housing may loosen and detach during use.
Elekta is recalling Leksell Gamma Knife radiosurgery systems, covering the Perfexion, Icon and Elekta Esprit models, due to an adapter not being properly aligned or locked in place.
Somerset Therapeutics is recalling one lot of Dexamethasone Sodium Phosphate Injection after out-of-specification impurity results at product expiry during long term stability testing.
Abbott is recalling one lot of the ID NOW Influenza A & B 2 test after confirming the lot has a higher occurrence of invalid rates than stated in the Instructions for Use.
Baxter is recalling the Welch Allyn Spot Vision Screener VS100 on software version 3.2.0.1 because the display screen may unintentionally flicker, which may induce photosensitive seizure activity.
ConvaTec is recalling two lots of the EsteemBody Drainable Pouch, REF 423643, because the drainable large pouch may leak due to a manufacturing issue.
GE Medical Systems is recalling Centricity Universal Viewer software versions 5.0 SP6 through 5.0 SP7.1 because user login credentials may be exposed on the local client workstation.
Diagnostica Stago is recalling the STA Liatest D-Di kit after investigations confirmed a positive bias in D-dimer measurements throughout the entire analytical range.