The Recall Desk

State

Minnesota product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44901–44925 of 81660

  • SevereNHTSA·17V834000·2017-12-21

    Maserati Recalls 2018 Quattroporte and Ghibli for Fuel Leak Risk

    Maserati is recalling 2018 Quattroporte and Ghibli vehicles because a fuel delivery pipe may leak, increasing the risk of a fire.

    Product
    MASERATI — MASERATI QUATTROPORTE, GHIBLI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18074·2017-12-21

    Brompton Recalls Folding Bicycles Due to Bottom Bracket Fall Hazard

    Brompton is recalling about 8,400 folding bicycles because the bottom bracket can break during use, posing a fall hazard. No injuries have been reported.

    Product
    Folding Brompton bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18072·2017-12-21

    Honda Recalls Portable Generators Due to Fire and Burn Hazards

    American Honda is recalling about 34,000 portable generators because a leaking carburetor poses fire and burn risks. No injuries have been reported.

    Product
    Honda portable generators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V824000·2017-12-21

    Chrysler Recalls Vehicles with Defective Kidde Fire Extinguishers

    Chrysler is recalling various Dodge, Jeep, and RAM vehicles equipped with specific Kidde fire extinguishers that may clog or detach, posing injury risks.

    Product
    DODGE — DODGE, RAM, JEEP DURANGO, CHALLENGER, RAM 1500, 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18070·2017-12-21

    Wohali Outdoors Recalls Children's Pajama Sets for Flammability Violations

    Wohali Outdoors is recalling about 26,800 children's three-piece pajama sets sold at Bass Pro Shops because they fail federal flammability standards, posing a risk of burn injuries.

    Product
    Children's three-piece pajama sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18709·2017-12-21

    John Deere Recalls Crossover Gator Utility Vehicles Due to Steering Loss

    John Deere is recalling about 68,300 Crossover Gator utility vehicles because the steering shaft can separate, causing a loss of steering control and posing a crash hazard.

    Product
    John Deere Crossover Gator™ utility vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V833000·2017-12-20

    Walker Recalls 2018 Tank Trailers Due to Brake Caliper Bolt Issues

    Walker is recalling 2018 Tank Trailers because improperly torqued brake caliper bolts may allow the caliper to detach, causing a loss of braking ability.

    Product
    WALKER — WALKER TANK TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V832000·2017-12-20

    Wabash National Truck Body Recall for Missing Weld on Support

    Wabash National is recalling 2018 Truck Body vehicles because a missing weld on the vertical leg support increases injury risk in rear-end collisions.

    Product
    WABASH NATIONAL — WABASH NATIONAL TRUCK BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V823000·2017-12-20

    Alfa Romeo Giulia and Stelvio Recalled for Brake Fluid Contamination

    FCA US LLC is recalling 2018 Alfa Romeo Giulia and Stelvio vehicles because contaminated brake fluid may damage the braking system and reduce performance.

    Product
    ALFA ROMEO — ALFA ROMEO GIULIA, STELVIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0109-2018·2017-12-20

    Sun Pharmaceutical Recalls Riomet Metformin Solution Due to Microbial Contamination

    Sun Pharmaceutical Industries is recalling Riomet (metformin hydrochloride) oral solution due to microbial contamination. The recall covers specific lots of the cherry-flavored prescription liquid.

    Product
    RIOMET — RIOMET (METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0186-2018·2017-12-20

    Physio-Control Recalls Defibrillation Electrodes Due to Incorrect Pad Placement Artwork

    Physio-Control is recalling 14,219 LIFEPAK defibrillation electrodes because the artwork instructs incorrect pad placement and is missing required warning symbols.

    Product
    LIFEPAK(R) defibrillation electrodes, Catalog # 11101-000016, MIN #3202380-006 The defibrillation electrodes are used only with LIFEPAK EXPRESS(R) AED, LIFEPAK CR(R) Plus AED, LIFEPAK 1000 defibrillator, or LIFEPAK 500 Biphasic AED s with a pink connector.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0187-2018·2017-12-20

    Physio-Control Recalls LIFEPAK Electrode Starter Kits Due to Labeling Errors

    Physio-Control is recalling 14,219 LIFEPAK Electrode Starter Kits because the infant artwork shows incorrect pad placement and is missing required warning symbols.

    Product
    LIFEPAK(R) Electrode Starter Kits, Catalog # 11101-000017, MIN #3202784-009 The defibrillation electrodes are used only with LIFEPAK EXPRESS(R) AED, LIFEPAK CR(R) Plus AED, LIFEPAK 1000 defibrillator, or LIFEPAK 500 Biphasic AED s with a pink connector.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V821000·2017-12-20

    FCA Recalls Ram Trucks Due to Transmission Shift Interlock Defect

    FCA is recalling specific Ram trucks because the brake transmission shift interlock pin may stick, allowing the vehicle to shift out of park without the brake pedal or key, increasing rollaway risk.

    Product
    RAM — RAM, DODGE 2500, 4500, 3500, RAM 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0252-2018·2017-12-20

    Navilyst Medical Recalls Xcela and BioFlo PICC Kits Due to Handle Detachment Risk

    Navilyst Medical is recalling specific Xcela and BioFlo PICC kits because the included introducer sheath handles may detach during use.

    Product
    Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved w/ Nit GW, UPN H965458950, Catalog No. 45-895 The Xcela with PASV, BioFlo PICC with ENDEXO Technology, and BioFlo PICC with ENDEXO and PASV Valve Technology are indicated for short or long-term peripheral access to the central…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V836000·2017-12-20

    Mobility Ventures Recalls MV-1 Vehicles for Seat Track Defect

    Mobility Ventures is recalling 2011-2016 MV-1 vehicles because the driver's seat may disengage from the track during a rear impact, increasing injury risk.

    Product
    MOBILITY VENTURES — MOBILITY VENTURES MV-1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0241-2018·2017-12-20

    Navilyst Medical Recalls Xcela and BioFlo PICC Kits Due to Handle Detachment

    Navilyst Medical is recalling Xcela and BioFlo PICC kits because the included Greatbatch introducer sheaths have handles that may detach during use.

    Product
    XCELA PASV 5F DL 55CM IR-145 Nitinol Wire KIT PG, UPN H965251260, Catalog No. 25-126 The Xcela with PASV, BioFlo PICC with ENDEXO Technology, and BioFlo PICC with ENDEXO and PASV Valve Technology are indicated for short or long-term peripheral access to the central venous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0242-2018·2017-12-20

    Navilyst Medical Recalls Xcela and BioFlo PICC Kits Due to Handle Detachment

    Navilyst Medical is recalling specific Xcela and BioFlo PICC kits because the included introducer sheaths have handles that may detach during use.

    Product
    XCELA PASV 5F DL 55CM MST-70 KIT PG, UPN H965457320, Catalog No. 45-732 The Xcela with PASV, BioFlo PICC with ENDEXO Technology, and BioFlo PICC with ENDEXO and PASV Valve Technology are indicated for short or long-term peripheral access to the central venous system for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0244-2018·2017-12-20

    Navilyst Medical Recalls Xcela and BioFlo PICC Kits Due to Handle Detachment

    Navilyst Medical is recalling Xcela and BioFlo PICC kits because the included introducer sheaths have handles that may detach during use.

    Product
    Bio-Stable 5F SL-55CM IR-145 Kit Valved PG, UPN H965458180, Catalog No. 45-818 The Xcela with PASV, BioFlo PICC with ENDEXO Technology, and BioFlo PICC with ENDEXO and PASV Valve Technology are indicated for short or long-term peripheral access to the central venous system…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17E078000·2017-12-20

    Eaton Cummins Transmission Recall for Unintended Vehicle Movement Risk

    Eaton Cummins is recalling specific Endurant and PACCAR transmissions where the control module may allow the engine to crank if the shifter is not in neutral, increasing crash risk.

    Product
    POWER TRAIN:AUTOMATIC TRANSMISSION:CONTROL MODULE (TCM/PCM/TECM) recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0445-2018·2017-12-20

    Frontier Trail Mix Recalled for Undeclared Milk Allergen

    Colorado Nut Co is recalling Frontier Trail Mix because it contains undeclared milk. Consumers with milk allergies should not eat the product.

    Product
    Frontier Trail Mix (4 oz. bag), UPC 018142352987. Packaged in Plastic Zip Lock bags. No refrigeration needed.
    Category
    Food
    Distribution
    24 states
  • HighFDA (Food)·F-0481-2018·2017-12-20

    Wegmans Dark Chocolate Cherry Cranberries Recalled for Undeclared Milk

    First Source, LLC is recalling Wegmans Dark Chocolate Cherry Infused Cranberries because the product contains undeclared milk.

    Product
    Wegmans Dark Chocolate Cherry Infused Cranberries 12 OZ (340g) tub UPC: 0 77890 33741 7
    Category
    Food
    Distribution
    23 states
  • HighFDA (Food)·F-0479-2018·2017-12-20

    First Source Recalls Dark Chocolate Almonds for Undeclared Milk

    First Source, LLC is recalling Dark Chocolate Almonds sold under multiple brands because the products contain undeclared milk.

    Product
    Dark Chocolate Almonds packaged under the brand names: (1)Wegmans, 23 OZ (1 LB 7 OZ) 652g tub UPC: 0 77890 328200 4 and 11.5 oz. (326g) tub UPC: 0 70784 50743 9; (2)Alpine Valley 11.5 OZ (326 g). tub UPC 0 23637 41099 8; (3)Tops 11.5oz . tub (326 g) UPC: 0 70784 50743 9; (4)…
    Category
    Food
    Distribution
    23 states