The Recall Desk

State

Minnesota product recalls

73,100 recalls have nationwide distribution and so reach Minnesota. 7,838 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total
7,838
Critical
1,139
Severe
1,904
Most recent
2026-09-23

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.

These figures cover only the 7,838 recalls whose distribution notice names Minnesota specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9526–9550 of 80938

  • SevereNHTSA·24V840000·2024-11-07

    Land Rover Recalls 2014-2016 Range Rovers for Suspension Defect

    Jaguar Land Rover is recalling 2014-2016 Range Rovers because a front suspension part may crack, risking loss of vehicle control.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25036·2024-11-07

    Smart Electric Space Heaters Recalled for Fire and Burn Hazards

    GoveeLife and Govee smart electric space heaters can overheat and pose fire and burn hazards due to non-compliance with UL 1278 safety standards. About 512,500 units are affected.

    Product
    GoveeLife and Govee Smart Electric Space Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V831000·2024-11-07

    Jayco Recalls 2024 Travel Trailers Due to Air Conditioner Fire Risk

    Jayco is recalling 2024 North Point and Pinnacle travel trailers because a faulty air conditioner component may overheat and cause a fire.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL PINNACLE, NORTH POINT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25038·2024-11-07

    Portable Lamps Recalled Due to Fire Hazard from Battery Overheating

    About 5,300 Tala Muse Portable Lamps are recalled due to fire hazard from battery overheating. One incident caused property damage; consumers should stop using the lamps and contact Tala for a free replacement bulb.

    Product
    Tala Muse Portable Lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25034·2024-11-07

    Wolf Dual Fuel ranges with infrared griddles recalled for fire and burn hazards

    Wolf Appliance is recalling about 44,000 Dual Fuel ranges with infrared griddles due to a short-circuit hazard. Liquid spillage can unexpectedly activate the griddle, posing burn and fire risks. No injuries have been reported.

    Product
    Wolf Dual Fuel ranges with infrared griddles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V843000·2024-11-07

    2024 Hyundai Santa Fe sunshade switch defect increases injury risk

    Hyundai is recalling 34,964 units of the 2024 Santa Fe and Santa Fe Hybrid with faulty switch knobs that may not retract, creating an injury risk.

    Product
    HYUNDAI — HYUNDAI SANTA FE HYBRID, SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25030·2024-11-07

    Dreamgro Lullaby Travel Soothers Recalled Due to Choking Hazard

    Dreamgro Lullaby mermaid travel soothers are recalled because a gold-colored soft star can detach, posing a choking hazard to infants. No injuries have been reported, but one detachment incident was confirmed.

    Product
    Dreamgro Lullaby mermaid travel soothers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V842000·2024-11-07

    Micro Bird Recalls 2023 CT-Series Buses Due to Ignition Interlock Defect

    Micro Bird is recalling 2023 CT-Series buses because the ignition interlock may allow the vehicle to start with the rear emergency door locked, increasing injury risk.

    Product
    MICRO BIRD — MICRO BIRD CT-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25031·2024-11-07

    Kyte Baby Slumber Suits Recalled Due to Flammability Violation, Burn Injury Risk

    Kyte Baby is recalling about 20,500 Slumber Suits sold from November 2022 to March 2024 because they violate federal flammability regulations for children's sleepwear, posing a risk of burn injuries. No injuries have been reported.

    Product
    Kyte Baby Slumber Suits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V841000·2024-11-07

    Micro Bird Recalls T-Series School Buses for Ignition Interlock Defect

    Micro Bird is recalling 2022-2024 T-Series school buses because the ignition interlock may allow the vehicle to start with the rear emergency door locked, increasing injury risk.

    Product
    MICRO BIRD — MICRO BIRD T-SERIES SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25033·2024-11-07

    Baofali 4-in-1 Microfiber Crib Bumpers Recalled for Suffocation Hazard

    Baofali 4-in-1 Microfiber Crib Safety Bumpers sold on Temu.com violate the federal crib bumper ban and pose a suffocation hazard to infants. About 390 units were sold from June through August 2024.

    Product
    Baofali 4-in-1 Microfiber Crib Safety Bumpers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V839000·2024-11-07

    2022-2023 Chevrolet Express and GMC Savana transmission software defect

    GM is recalling 2022-2023 Chevrolet Express and GMC Savana vehicles for a transmission software defect that may cause rear wheel lockup and unintended vehicle movement. Dealers will update the software free of charge.

    Product
    GMC — GMC, CHEVROLET SAVANA, EXPRESS, EQUINOX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25032·2024-11-07

    Guava Roam strollers recalled due to brake failure and fall hazards

    Guava Roam strollers are recalled because the brakes can fail to engage or unexpectedly disengage, posing fall and injury hazards to children. No injuries have been reported.

    Product
    Guava Roam Strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0128-2025·2024-11-06

    Dakota Toms Bacon Cheeseburger Recalled for Potential Listeria Contamination

    Dakota Toms Bacon Cheeseburger (5.7 oz) is being recalled due to potential Listeria monocytogenes contamination. The recall affects 1700 sandwiches distributed in North Dakota, South Dakota, Wyoming, Iowa, and Minnesota with expiration dates from September 1 through November 28, 2024.

    Product
    Bacon Cheeseburger , Dakota Toms brand, Net Wt 5.7 oz, individual pre-packaged components in MEP packaging, UPC 737296803007
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0129-2025·2024-11-06

    Dakota Tom's The Gambler Sandwiches Recalled for Potential Listeria Contamination

    Dakota Tom's The Gambler sandwiches are recalled for potential Listeria monocytogenes contamination. Products were distributed to retail locations in ND, SD, WY, IA, and MN, with expiration dates September 1–November 28, 2024.

    Product
    The Gambler, Dakota Toms brand, Net Wt 7.8 oz, individual pre-packaged components in MEP packaging, UPC 737296601788
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-0208-2025·2024-11-06

    Phasitron5 breathing circuits recalled for nickel-coated spring discoloration

    Percussionaire Corporation is recalling Phasitron5 breathing circuits (P5-10, P5-HC, P5-UC-10) due to discolored fluid caused by an unintended nickel coating on the spring component reacting with medicated mist. 43,830 devices have been distributed across the U.S.

    Product
    Phasitron5 Breathing Circuit (P5-10, P5-HC, P5-UC-10). component of Intrapulmonary Percussive Ventilation, used to provide airway clearance therapy
    Category
    Medical Device
    Distribution
    40 states
  • SevereFDA (Food)·F-0073-2025·2024-11-06

    Jack & the Green Sprouts Alfalfa Recalled for Possible Listeria Contamination

    Jack & the Green Sprouts Alfalfa sprouts (5 oz containers) are being recalled due to potential Listeria monocytogenes contamination. Affected products were distributed in Iowa, Minnesota, and Wisconsin.

    Product
    Jack & the Green Sprouts Alfalfa, Net Weight 5 oz (142g). UPC 7 63247-19891 5 Keep Refrigerated. Product of USA. Jackandthegreensprouts.com, River Falls, WI 54022. EXPANDED 10/4/2024: Product was packaged in 5 oz containers that were packed in 6 count or 12 count…
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0074-2025·2024-11-06

    Jack & the Green Sprouts Alfalfa & Onion recalled for Listeria

    Jack & the Green Sprouts Alfalfa & Onion is being recalled due to potential Listeria monocytogenes contamination. Affected lot 300 with expiration date 10/9/24 should be discarded.

    Product
    Jack & the Green Sprouts Alfalfa & Onion, Net Weight 5 oz (142g). UPC 7 63247-19594 5 Keep Refrigerated. Product of USA. Jackandthegreensprouts.com, River Falls, WI 54022
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0127-2025·2024-11-06

    Pepperjack Cheese Burger Recalled for Potential Listeria Contamination

    Dakota Toms Pepperjack Cheese Burgers are recalled for potential Listeria monocytogenes contamination. Affected products expire between 9/1/24 and 11/28/24.

    Product
    Pepperjack Cheese Burger, Dakota Toms brand, Net Wt 5.7 oz, individual pre-packaged components in MEP packaging, UPC 737296806008
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·24V837000·2024-11-06

    PJ TRAILERS LD trailers recalled for incorrectly installed brake axles

    PJ TRAILERS is recalling certain 2024-2025 LD trailers because air ride suspension brake axles may be installed incorrectly. This could reduce braking ability and increase the risk of crashes.

    Product
    PJ TRAILERS — PJ TRAILERS LD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0092-2025·2024-11-06

    VasoView HemoPro Vessel Harvesting System Recalled for Silicone Component Detachment

    Maquet Cardiovascular is recalling the VasoView HemoPro Endoscopic Vessel Harvesting System due to silicone detachment from the Harvesting Tool Jaws during use. This FDA Class I recall affects 28,809 units worldwide.

    Product
    VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0032-2025·2024-11-06

    Cinacalcet 90 mg Tablets Recalled for Nitrosamine Impurity Above Safety Limits

    Accord Healthcare is recalling Cinacalcet 90 mg tablets nationwide due to nitrosamine impurity (N-nitroso-cinacalcet) at levels exceeding the FDA's acceptable daily intake limit. The issue stems from manufacturing process deviations.

    Product
    CINACALCET — CINACALCET (CINACALCET)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0247-2025·2024-11-06

    Surgical patties and strips recalled for elevated endotoxin levels

    Integra LifeSciences is recalling surgical patties and strips (Model 801409) used in surgery due to higher-than-expected endotoxin levels detected in raw materials. No illnesses have been reported.

    Product
    SURG PAT XRAY 3X3 Model/Catalog Number: 801409. The surgical patties and surgical strips are indicated for the use in protection of tissue, including brain and other tissues of the central nervous system, during surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0239-2025·2024-11-06

    Surgical Patties and Strips Recalled for Out-of-Specification Endotoxin

    Integra LifeSciences is recalling Codman Surgical Patties and Strips (Model 801400) due to higher-than-expected endotoxin levels in raw materials that resulted in out-of-specification finished products.

    Product
    SURG PAT XRAY 1/2X1/2 Model/Catalog Number: 801400. The surgical patties and surgical strips are indicated for the use in protection of tissue, including brain and other tissues of the central nervous system, during surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide