The Recall Desk

State

Minnesota product recalls

73,817 recalls have nationwide distribution and so reach Minnesota. 7,851 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total
7,851
Critical
1,137
Severe
2,246
Most recent
2026-11-04

Of the 7,851 recalls naming Minnesota we have scored against our rubric, 1,137 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,246 (29%) are Severe.

These figures cover only the 7,851 recalls whose distribution notice names Minnesota specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47051–47075 of 81668

  • SevereCPSC·17195·2017-07-25

    Polaris Recalls RZR 170 Vehicles Due to Fuel Leak and Fire Hazards

    Polaris is recalling 16,800 RZR 170 recreational off-highway vehicles because fuel tank necks can crack or wiring can overheat, posing fire risks.

    Product
    RZR 170 recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V472000·2017-07-25

    Ford Recalls 2014-2015 Vehicles Due to Improper Seat Bolts

    Ford is recalling 94,605 vehicles because improperly manufactured bolts may fracture, increasing injury risk in a crash.

    Product
    FORD — FORD, LINCOLN ESCAPE, F-150, E-350, MKC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·085-2017·2017-07-25

    D & D Foods Recalls Pepperoni Pizza Due to Undeclared Soy Allergen

    D & D Foods is recalling approximately 17,847 pounds of Hy-Vee pepperoni pizza products because they contain undeclared soy lecithin, a known allergen.

    Product
    D & D Foods, Inc. Recalls Pizza Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·17193·2017-07-24

    iRover Recalls Self-Balancing Scooters Due to Fire and Explosion Hazard

    iRover is recalling about 2,800 self-balancing scooters because their lithium-ion batteries can overheat, smoke, catch fire, or explode. No injuries or property damage have been reported.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V468000·2017-07-22

    Piaggio Recalls 2014-2017 Fly 150 3V Scooters for Brake Defect

    Piaggio is recalling 2014-2017 Fly 150 3V scooters because front brake disc mounting screws may loosen, potentially causing the front wheel to lock up and increasing crash risk.

    Product
    PIAGGIO — PIAGGIO FLY 150 3V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V467000·2017-07-21

    BMW Recalls 2017 C Evolution and C650 GT Scooters for Rim Marking Defect

    BMW is recalling 2017 C Evolution and C650 GT scooters because front rims may lack required markings, which could lead to incorrect tire installation and handling issues.

    Product
    BMW — BMW C EVOLUTION, C650 GT MAXI-SCOOTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V464000·2017-07-20

    Tremcar Recalls Rear Impact Guards on Certain Trailers

    Tremcar is recalling rear impact guards on specific trailers because they may not adequately resist force in a crash, increasing the risk of injury.

    Product
    TREMCAR — TREMCAR 1625FT3 VAC TANDEM, 2800FT3 DRY BULK QUAD, 1350FT3 B-TRAIN PUP, 2300FT3 QUAD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V460000·2017-07-20

    Spartan Motors Recalls 2015-2017 Aeromaster Vehicles for Wiper Motor Defect

    Spartan Motors is recalling 2015-2017 Utilimaster Aeromaster vehicles because a missing ground wire may cause intermittent loss of windshield wiper function, increasing crash risk.

    Product
    UTILIMASTER — UTILIMASTER AEROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0970-2017·2017-07-19

    FDA Recalls ZRECT for Women Herbal Supplement Due to Undeclared Drugs

    Organic Herbal Supply is recalling ZRECT for Women herbal capsules because FDA testing found undeclared prescription drugs, including tadalafil and sildenafil.

    Product
    ZRECT for Women Herbal Dietary Supplement Capsules, 500 mg, supplied in 30 count packages, Distributed by Organic Herbal Supply, Roseville, CA --- UPC Code 680474229055
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0961-2017·2017-07-19

    UPROAR Male Enhancement Supplement Recalled for Undeclared Prescription Drugs

    Organic Herbal Supply is recalling UPROAR male enhancement capsules because FDA testing found undeclared prescription drugs, including tadalafil and sildenafil.

    Product
    UPROAR All Natural Male Enhancement Herbal Dietary Supplement Capsules, supplied in 2, 4 and 10 count packages, Distributed by AH Distribution, DelRay, Beach, FL ---- UPC Code 680474229260
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2541-2017·2017-07-19

    Wildway Coconut Cashew Granola Recalled for Listeria Risk

    Wildway LLC is recalling specific lots of Coconut Cashew Grain-free Granola due to potential contamination with Listeria monocytogenes.

    Product
    Wildway Coconut Cashew Grain-free Granola 8 oz. and 10 oz. UPC: 858660005183 packaged in a plastic bag
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0965-2017·2017-07-19

    Rectalis Male Enhancement Supplement Recalled for Undeclared Prescription Drugs

    Organic Herbal Supply is recalling Rectalis Male Enhancement Capsules because FDA analysis found undeclared prescription drugs, including tadalafil and sildenafil.

    Product
    RECTALIS Male Enhancement Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Made in Malaysia, Distributed by Organic Herbal Supply, Cheyenne, WY --- UPC Code 680474228782
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0964-2017·2017-07-19

    Xrect Male Enhancement Supplement Recalled for Undeclared Prescription Drugs

    Organic Herbal Supply is recalling Xrect Male Enhancement capsules because FDA analysis found undeclared prescription drugs tadalafil, sildenafil, and Flibanserin.

    Product
    Xrect Male Enhancement Herbal Dietary Supplement Capsules, 500 mg supplied in 2, 4 and 10 count packages, Distributed by Organic Herbal Supply, Roseville, CA ---- UPC Code 680474015795
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0969-2017·2017-07-19

    Enhancerol Herbal Supplement Recalled for Undeclared Prescription Drug Ingredients

    Organic Herbal Supply is recalling Enhancerol Herbal Dietary Supplement Capsules because FDA analysis found undeclared tadalafil, sildenafil, and Flibanserin.

    Product
    ENHANCEROL Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Made in Malaysia, Distributed by Organic Herbal Supply, Cheyenne, WY ---- UPC Code 680474229086
    Category
    Drug
    Distribution
    Distributed nationwide