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.

Which agencies issued them

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.

45176–45200 of 81660

  • HighFDA (Food)·F-0338-2018·2017-11-22

    Aurora Dark Chocolate Almonds Recalled for Undeclared Milk

    Aurora Products is recalling Dark Chocolate Almonds nationwide and in Bermuda because the product contains undeclared milk.

    Product
    Dark Chocolate Almonds packaged in: 4 oz. Plastic Pouch, 9 oz. Plastic Cup, 9 oz. Stand Up Plastic Pouch, 12 oz. Square Plastic Tub, 17 oz. Family Size Plastic Pouch. Aurora Brand and Store Branded Labeling Include: AG Supermarkets, Belmont Market, Boiceville Market…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V765000·2017-11-22

    KME Fire Trucks Recalled for Pressure Valve Defect

    KME is recalling 74 fire trucks because corroding rings may cause pressure relief valves to open, reducing water pressure for firefighting.

    Product
    KME — KME PREDATOR SS TANKER, PREDATOR SS PUMPER, PREDATOR SS AERIAL, COMMERCIAL PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0342-2018·2017-11-22

    Aurora Dark Chocolate Almonds Recalled for Undeclared Milk

    Aurora Products is recalling Dark Chocolate Turbinado Almonds with Sea Salt because the product contains undeclared milk. The recall affects 1,128 units distributed nationwide and in Bermuda.

    Product
    Dark Chocolate Turbinado Almonds w/ Sea Salt packaged in : 7 oz. Plastic Cup Packaged under the following: Aurora Brand and Store Branded Labeling Include: Gourmet Garage, Lee's Supermarket
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0101-2018·2017-11-22

    ICU Medical Recalls Plum 360 Infusion Systems Due to Software Malfunction

    ICU Medical is recalling 21,461 Plum 360 Infusion Systems because a software defect can prevent users from stopping the pump or restarting delivery under specific conditions.

    Product
    Plum 360 Infusion System, List number 30010.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0340-2018·2017-11-22

    Aurora Dark Chocolate Cranberries Recalled for Undeclared Milk

    Aurora Products is recalling Dark Chocolate Cranberries because the product contains undeclared milk, a major food allergen.

    Product
    Dark Chocolate Cranberries packaged in: Bulk 3.5 oz. Plastic Cup 4.75 oz. Plastic Pouch 9 oz. Plastic Cup 9 oz. Plastic Pouch 11 oz. Square Plastic Tub 18 oz. Family Size Plastic Pouch 26 oz. Plastic Tray Aurora Brand and Store Branded Labeling Include: AG…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V751000·2017-11-22

    Cruiser RV Recalls Vehicles with Defective Kidde Fire Extinguishers

    Cruiser RV is recalling specific recreational vehicles equipped with certain Kidde fire extinguishers that may clog or have nozzles detach, posing injury risks during a fire.

    Product
    CRUISER RV — CRUISER RV STRIKER, SHADOW CRUISER ULTRA LITE, SHADOW CRUISER LE, SHADOW CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V758000·2017-11-22

    Thor Motor Coach Recalls RVs with Defective Kidde Fire Extinguishers

    Thor Motor Coach is recalling 2003-2018 recreational vehicles equipped with specific Kidde fire extinguishers that may clog or detach, increasing injury risk during a fire.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR, FOUR WINDS VENTURA, TUSCANY XTE, FREEDOM ELITE, FOUR WINDS SIESTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V755000·2017-11-22

    Keystone Recalls Recreational Trailers with Defective Kidde Fire Extinguishers

    Keystone RV is recalling 2003-2018 Crossroads, Dutchmen, and Keystone trailers because the installed Kidde fire extinguishers may clog or detach, posing injury risks during a fire.

    Product
    DUTCHMEN — DUTCHMEN, KEYSTONE, CROSSROADS T@B, SPORT, SKAMPER, IMPACT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V756000·2017-11-22

    Forest River and Coachmen Recalling RVs with Defective Fire Extinguishers

    Forest River is recalling 2003-2018 motorhomes and trailers equipped with certain Kidde fire extinguishers that may clog or detach, increasing injury risk during a fire.

    Product
    COACHMEN — COACHMEN, SHASTA, CARGO MATE FREEDOM EXPRESS, OASIS, REVERE, CARGO MATE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0341-2018·2017-11-22

    Aurora Dark Chocolate Coffee Beans Recalled for Undeclared Milk

    Aurora Products is recalling Dark Chocolate Coffee Beans in various package sizes due to undeclared milk. The recall covers products distributed nationwide and in Bermuda.

    Product
    Dark Chocolate Coffee beans packaged in Bulk 4 oz. Plastic Pouch 8.25 oz. Plastic Pouch 8.25 oz. Plastic Cup 17 oz. Family Size Plastic Pouch Aurora Brand and Store Branded Labeling Include: AG Supermarkets, Belmont Market, Boiceville Market, Deciccos, Grauls Market…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0079-2018·2017-11-22

    Fagron Recalls Estriol Compounding Powder Due to Quality Assurance Deviations

    Fagron, Inc. is recalling Estriol for prescription compounding due to lack of quality assurance at the API manufacturer.

    Product
    Estriol, For Prescription Compounding, packaged in a) 1 G bottle (NDC: 51552-1392-1), b) 5 G bottle (NDC: 51552-1392-2), c) 25 G bottle (NDC: 51552-1392-3) and d) 100 G bottle (NDC 51552-1392-5), Rx only, Distributed by Fagron, Inc., 2400 Pilot Knob Rd, St. Paul, MN 55120 Tel.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0098-2018·2017-11-22

    Karl Storz Recalls Mislabeled High Flow Insufflation Tubing Pouches

    Karl Storz Endoscopy is recalling 496 boxes of High Flow Insufflation Tubing because some inner pouches are mislabeled with the wrong catalog number.

    Product
    STORZ High Flow Insufflation Tubing (with filter), Catalog #20400161S/10 (outer box label), ENDOFLATOR 26-430520-1 also referenced on outer box), individually packaged in a sterile pouch (Catalog #20400161S), 10 pouches per cardboard box. Some of the pouches inside of cardboard…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0074-2018·2017-11-22

    Amerisource Recalls Enalapril Maleate Tablets Due to Stability Failures

    Amerisource Health Services is recalling Enalapril Maleate Tablets, 5 mg, because the product failed stability specifications.

    Product
    Enalapril Maleate Tablets, USP, 5 mg, 100 Tablets (10 x 10), Rx Only. Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC: 68084-390-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0077-2018·2017-11-22

    Allergan Recalls Combigan Eye Drops Due to Failed Impurity Specifications

    Allergan is recalling 715,041 bottles of Combigan ophthalmic solution because the product failed impurities and degradation specifications.

    Product
    COMBIGAN — COMBIGAN (BRIMONIDINE TARTRATE, TIMOLOL MALEATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0075-2018·2017-11-22

    Genzyme Recalls Clolar Injection Due to Missing Package Insert

    Genzyme Corporation is recalling Clolar (clofarabine) injection vials because the package insert is incorrect or missing.

    Product
    Clolar (clofarabine) 20 mg/20 mL (1 mg/mL) Injection, for intravenous use, Rx Only, Mfd. by: Teva Pharmachemie Swensweg 5 Haarlem, The Netherlands Mfd. for: Genzyme Corporation, Cambridge, MA 02142, NDC 0024-5860-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalCPSC·18040·2017-11-21

    IKEA Recalls Chests and Dressers Due to Serious Tip-Over Hazard

    IKEA is reannouncing a recall of MALM and other chests and dressers due to tip-over hazards that have resulted in eight child fatalities.

    Product
    Children's and adult chests and dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V741000·2017-11-21

    Chrysler Recalls 2014 Models for Alternator Failure Risk

    Chrysler is recalling 17,116 2014 Dodge, Jeep, and Chrysler vehicles because the alternator may fail, causing the vehicle to stall without warning.

    Product
    JEEP — JEEP, CHRYSLER, DODGE GRAND CHEROKEE, 300, CHALLENGER, CHARGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V732000·2017-11-21

    Jeep Recalls 2018 Compass Models Due to Loose Air Bag Mounting Nuts

    Chrysler is recalling 2018 Jeep Compass vehicles because loose passenger air bag inflator nuts could become projectiles in a crash, posing a risk of serious injury or death.

    Product
    JEEP — JEEP COMPASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·18044·2017-11-21

    Plycem Recalls Allura Decking Due to Fall and Injury Hazards

    Plycem is recalling Allura fiber cement decking and fascia because the materials can crack, causing consumers to fall through and suffer injuries.

    Product
    Allura decking
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17E069000·2017-11-21

    Volvo Recalls Kidde Fire Extinguishers for Clogging and Detachment Risks

    Volvo Trucks North America is recalling Kidde plastic-handle fire extinguishers sold as accessories for Volvo trucks. The units may clog, require excessive force to activate, or have nozzles detach, posing injury risks.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide