State
72,940 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 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Olympus is recalling its Resection Inner Sheath for 26 Fr outer sheath, model A22040A, used in urologic applications, after complaints that the ceramic tip can break.
Vista Gonio Eye Lubricant eye drops are being recalled because they may not be sterile. The product was not manufactured according to proper sterile drug-making standards.
Medtronic is recalling one lot of the Octopus Nuvo Tissue Stabilizer after identifying an assembly issue in which the short and long tubes were attached to the wrong ends of the canister.
Olympus recalls 91 units of its Inner Sheath Model A4741 medical device after receiving complaints of the ceramic tip breaking during gynecological endoscopic procedures.
Medline is recalling five Trunk Kit convenience kits because the manufacturer of the sterile saline wound wash they contain may not have met the required sterility assurance level.
Agiliti Health - Ellis is recalling Adapt Pumps (Model 61600200) because the Microclimate Management function may fail to re-engage after using the Autofirm function.
Edermy LLC is recalling the PIE Trolley System, model 2005, because the device lacks 510(k) clearance from the FDA.
SB FOOD LLC is recalling Yoyo Gummy Tropical Flavor candy because it contains Carmoisine (E122), a color additive not approved for use in this product. The recalled product was distributed to 15 states.
Edermy LLC is recalling PIE PAK models P2HC-A, P2HC-S and P2HC because the devices lack 510(k) clearance from the FDA.
SB FOOD LLC is recalling Yoyo Gummy Assorted Flavor because the product contains Carmoisine (E122) - Acid Red 14, which is an unallowed color.
Slate Run Pharmaceuticals is recalling Eptifibatide Injection due to a labeling error on the carton, which incorrectly describes the dosing instructions.
Ajinomoto Foods North America is expanding a recall for frozen fried rice, ramen, and shu mai products due to possible glass contamination. No injuries have been reported.
Ford Motor Company is recalling certain 2025 and 2026 F-250 SD and F-350 SD vehicles due to a potential driveshaft failure that could lead to a loss of power.
Ford Motor Company is recalling certain 2020-2022 Ford and Lincoln vehicles because the windshield wiper motors may fail, potentially reducing visibility and increasing crash risks.
Ford Motor Company is recalling certain 2025-2026 Explorer vehicles because the headlight system software may cause the passenger-side headlight to turn in the wrong direction during curves.
Ford is recalling certain 2025 vehicles due to a potential EGR valve failure that could cause an unexpected loss of drive power, increasing crash risk.
Ford is recalling certain 2021-2026 Bronco and 2021-2024 Edge vehicles because the rearview camera may fail to display an image due to an overheating module.
Ford Motor Company is recalling certain 2020-2024 Lincoln and Ford vehicles because the center display may show an inverted rearview image, increasing crash risks.
Ford Motor Company is recalling certain 2026-2027 E-350 and E-450 vehicles because the backup alarm may fail to sound, increasing the risk of a crash.
Ford is recalling 2026 Lincoln Navigator vehicles because the driver seat software may malfunction at low speeds, causing the seat to move unexpectedly and increasing crash risk.
USDA FSIS issued a public health alert for Punahele beef jerky products containing undeclared soy lecithin. Consumers are advised not to consume the items.
TheKiddoSpace is recalling its Children's Montessori Egg Puzzle Toys due to a choking hazard. The recalled toys are intended for children under three years of age and the eggs can block a child's airway, posing a risk of choking and death to children.
Royal Oak Enterprises is recalling approximately 190,560 Flame Saber Lighters because they lack required child-resistant mechanisms, posing a risk of serious injury or death.
Trankerloop is recalling approximately 2,380 baby bath seats because they are unstable and can tip over, posing a risk of serious injury or death from drowning.
Grtard is recalling approximately 130 Grtard Magnet Stick Figure Men Toy Sets because they contain loose magnets that pose a serious injury or death risk if swallowed.