State
20,199 recalls have nationwide distribution and so reach Minnesota. 0 additional recalls listed Minnesota specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Minnesota consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
Cardinal Healthcare is recalling Allopurinol 300 MG tablets (batch L100813) nationwide because products were exposed to temperatures outside their labeled storage conditions. Patients should consult their healthcare provider.
Cardinal Healthcare is recalling Asmanex Twisthaler inhalers (batch U027458) because they were exposed to temperatures outside their labeled storage conditions. The FDA classified this as a Class II recall due to the manufacturing deviation.
CARDINAL HEALTHCARE is recalling Amoxicillin for Oral Suspension nationwide due to CGMP deviations. Products were exposed to temperatures outside their labeled storage conditions.
General Motors is recalling certain 2020-2024 Chevrolet Silverado and GMC Sierra pickup trucks due to faulty electronic tailgate switches that may inadvertently unlatch while the vehicle is parked. The defect can allow the tailgate to open while driving, potentially causing cargo loss and creating a road hazard.
Proterra is recalling certain 2020–2022 Catalyst and ZX5 buses due to windshield wiper motor failure. Inoperative wipers reduce visibility and increase crash risk.
Hyundai is recalling 2023 IONIQ 5, IONIQ 6, and Genesis GV60 vehicles for rear driveshafts that may break under load due to improper heat treatment, causing loss of drive power. Dealers will replace the driveshaft free of charge.
Jayco is recalling certain 2020-2023 Entegra motorhomes because passenger seats may have improperly welded pedestals that can separate and cause the seat to loosen or detach.
Honda and Acura are recalling 750,114 vehicles from 2020-2022 model years. A defective front passenger seat weight sensor may fail to suppress the airbag, increasing the risk of injury in a crash.
Tiffin is recalling certain 2022–2024 Allegro Bay motorhomes because batteries may shift during travel, causing electrical arcing and fire risk. Dealers will install new hold-down hardware at no charge.
ABS Remorques is recalling 2014-2023 RC, WC, LRC, and LWC semi-trailers due to coupling plate deterioration that may cause king pin failure and trailer detachment. Detached trailers cannot be controlled and may crash or obstruct traffic.
Certain 2021 Harley-Davidson motorcycles may not display the speedometer or neutral indicator at startup in freezing temperatures, creating a crash risk. Owners should contact Harley-Davidson for a free software update.
A set of 5mm magnetic balls sold online through Walmart.com via Joybuy is being recalled because the magnets are too strong and can cause serious internal injuries or death if swallowed, especially by children.
BlendJet Inc. is recalling approximately 4.8 million BlendJet 2 Portable Blenders because they can overheat, catch fire, or have blades that break off during use, creating fire and laceration hazards.
FNA Group is recalling about 2,930 Simpson Gas Pressure Washers with Electric Start because the lithium battery in the electric start system can overheat and pose a burn hazard. Two reports of battery overheating have been received, but no injuries have been reported.
Raw Seafoods Inc. is recalling frozen, lightly seasoned salmon burgers nationwide due to undeclared sesame seeds and milk, which pose serious allergic reaction risk to sensitive consumers.
Nurse Assist, LLC is recalling sterile water and saline bottles across multiple brands due to potential lack of sterility assurance. The products could be nonsterile and may cause infection.
Nurse Assist is recalling sterile water and saline irrigation products due to lack of sterility assurance. Use of nonsterile products could result in infection.
The FDA recalled Phenytoin Oral Suspension from Major Pharmaceuticals due to failed content uniformity specifications affecting 3,718 units distributed nationwide.
ResMed is recalling the AirFit F30 Full Face Mask because the device contains magnets that can interfere with active medical implants and ferromagnetic objects. The original user guide did not adequately warn about safe distance requirements.
Insight Pharmaceuticals recalls TING 2% Miconazole Nitrate Athlete's Foot Spray due to benzene contamination. The recall affects 117,336 cans distributed nationwide and in Puerto Rico.
ResMed is recalling the AirFit F30i Full Face Mask due to potential magnetic interference with active medical implants and ferromagnetic objects. Safety warnings are being updated.
ResMed is recalling 424,309 units of AirTouch N20 Nasal Masks because they contain magnets that may interfere with active medical implants and ferromagnetic materials. Updated safety warnings are being provided.
ResMed is recalling AirFit F20 Full Face Masks due to magnets that can interfere with active medical implants. Updated warnings will guide safe distances for patients and those in close contact.
Nurse Assist, LLC recalls sodium chloride irrigation solutions and IV flush syringes due to potential lack of sterility assurance, which could allow contamination and infections.
Blistex Inc is recalling Odor-Eaters brand Tolnaftate 1% antifungal spray powder nationwide due to benzene contamination. The recall affects approximately 243,386 cases distributed in the USA, Canada, and Korea.