The Recall Desk

State

Minnesota product recalls

73,576 recalls have nationwide distribution and so reach Minnesota. 7,844 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total
7,844
Critical
1,139
Severe
2,243
Most recent
2026-10-24

Of the 7,844 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 2,243 (29%) are Severe.

These figures cover only the 7,844 recalls whose distribution notice names Minnesota specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25301–25325 of 81420

  • SevereNHTSA·21V858000·2021-11-04

    Volvo Recalls 2021 VNL Trucks Due to Power Steering Pump Defect

    Volvo Trucks North America is recalling 2021 VNL vehicles because a machining defect in the power steering pump may cause a loss of steering assist, increasing crash risk.

    Product
    VOLVO — VOLVO VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22705·2021-11-04

    Kubota RTV-X1100C Utility Vehicles Floor Mat Interference Recall

    Kubota is recalling about 48,875 RTV-X1100C utility vehicles from model years 2013 through 2021 because floor mats can warp or degrade and interfere with the throttle pedal, creating crash and injury risks.

    Product
    Kubota RTV-X1100C Model Utility Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V857000·2021-11-04

    Tracker Recalls 2022 Ranger Trail Boat Trailers Due to Fender Spacing

    Tracker Marine is recalling 2022 Ranger Trail boat trailers because improperly spaced fenders may contact tires, causing premature wear and potential tire failure.

    Product
    RANGER TRAIL — RANGER TRAIL BOAT TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22706·2021-11-04

    Backyard Play Systems Outdoor Playsets Recalled for Entrapment Hazard

    Backyard Play Systems is recalling four outdoor playset models due to an entrapment hazard in the wooden roof design. Children can become trapped in gaps between the roof structure and gable decoration.

    Product
    Turbo Racer, Cloud Racer, Captain's Fort and Fort Highlander Outdoor Playsets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0118-2022·2021-11-03

    Surgical Brain Guidance System Recalled for Inaccurate Electrode Placement

    ROSA One 3.1 surgical guidance system recalled due to a software anomaly causing inaccurate electrode placement during brain and spine surgery. Manufacturer received 3 complaints related to the issue.

    Product
    ROSA One 3.1 Brain application The device is intended for the spatial positioning and orientation of instruments holders or tool guides to be used by trained surgeons to guide standard surgical instruments during brain and spine surgeries.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0046-2022·2021-11-03

    Test Cyp Injectable Drug Recalled for Sterility Assurance Defects

    First Royal Care Compounding Pharmacy is recalling Test Cyp 50mg/ml in ethyl oleate oil due to FDA inspection findings that raised concerns about sterility assurance. About 494 patients in seven states received prescriptions for the affected product.

    Product
    TEST CYP 50MG/ML IN ETHYL OLEATE OIL, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0053-2022·2021-11-03

    Acetylcysteine 10% ophthalmic solution recalled for sterility assurance concerns

    Red Mountain Compounding Pharmacy is recalling Acetylcysteine 10% ophthalmic solution due to lack of sterility assurance identified during an FDA inspection. Approximately 494 patients received prescriptions for the product across seven states.

    Product
    ACETYLCYSTEINE 10% OPTH SOLN, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0030-2022·2021-11-03

    Levocarnitine 100mg/mL Solution Recall Due to Sterility Assurance

    Red Mountain Compounding Pharmacy is recalling Levocarnitine 100mg/mL solution for injection because FDA inspection found concerns about the product's sterility assurance. The product was distributed to patients in seven states.

    Product
    LEVOCARNITINE 100MG/ML MDV SOLN, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0037-2022·2021-11-03

    Estradiol Valerate Injection Recalled for Sterility Assurance Concerns

    Red Mountain Compounding Pharmacy is recalling Estradiol Valerate 5mg/mL injectable medication due to FDA inspection findings of inadequate sterility assurance. The product was distributed to approximately 494 patients across seven states.

    Product
    ESTRADIOL VALERATE 5MG/ML MDV INJ, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0066-2022·2021-11-03

    Progesterone 100mg/ml Oil Injection Recall: Sterility Assurance Defect

    Red Mountain Compounding Pharmacy is recalling Progesterone 100mg/ml MDV Oil Injection due to lack of assurance of sterility following FDA inspection. About 494 patients in seven states received prescriptions for this affected product.

    Product
    PROGESTERONE 100MG/ML MDV OIL INJECTION, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0065-2022·2021-11-03

    MIT/B12 Compounded Injection Recalled for Sterility Assurance Concerns

    Red Mountain Compounding Pharmacy is recalling MIT/B12 25/50/50MG/ML 1MG/ML multidose vials due to FDA inspection findings that raised concerns about the lack of assurance of sterility. The product was distributed to approximately 494 patients across seven states.

    Product
    MIT/B12 25/50/50MG/ML 1MG/ML MDV, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0035-2022·2021-11-03

    Cyclosporine 2% MCT Oil Suspension Recalled for Sterility Assurance

    Red Mountain Compounding Pharmacy is recalling Cyclosporine 2% MCT Oil Suspension due to FDA inspection findings of sterility assurance concerns. Approximately 494 patients in seven states received prescriptions for this medication.

    Product
    CYCLOSPORINE 2% MCT OIL SUSP, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Food)·F-0072-2022·2021-11-03

    Nature's Heart Toasted Coconut Chips recalled for undeclared peanuts

    Nestle USA is recalling Nature's Heart Toasted Coconut Chips 1.5oz pouches because they contain undeclared peanuts, posing a serious risk to consumers with peanut allergies.

    Product
    Nature's Heart Toasted Coconut Chips 1.5oz poly film pouches - 32 units per case
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Drugs)·D-0048-2022·2021-11-03

    Compounded Anabolic Steroid Product Recalled for Sterility Assurance Concerns

    Red Mountain Compounding Pharmacy is recalling a compounded anabolic steroid product due to FDA concerns about sterility assurance identified during inspection. The product was distributed to approximately 494 patients in seven states.

    Product
    TEST CYP/PROP/DECA-NAN 125MG/ML (80/10/10) IN SESAME OIL, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0039-2022·2021-11-03

    Hydroxyprogesterone Caproate Injection Recalled Due to Sterility Concerns

    First Royal Care Compounding Pharmacy is recalling Hydroxyprogesterone Caproate 250 mg/mL oil injection due to lack of assurance of sterility identified during FDA inspection. The drug was distributed to patients in seven states.

    Product
    HYDROXYPROG CAPROATE 250MG/ML OIL INJ, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0028-2022·2021-11-03

    Calcium Chloride Injection Recalled Due to Sterility Assurance Concerns

    Red Mountain Compounding Pharmacy is recalling Calcium Chloride 100 mg/mL multi-dose vial injection due to lack of assurance of sterility identified during FDA inspection. The product was distributed to approximately 494 patients across seven states.

    Product
    Calcium Chloride, 100 mg/mL MDV INJ, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0044-2022·2021-11-03

    TEST CYP 200MG/ML injection recalled due to sterility assurance concerns

    Red Mountain Compounding Pharmacy is recalling TEST CYP 200MG/ML MDV ETHYL OLEATE due to FDA inspection findings of lack of assurance of sterility. The product was distributed to approximately 494 patients across seven states.

    Product
    TEST CYP 200MG/ML MDV ETHYL OLEATE, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0038-2022·2021-11-03

    Glutathione 200mg/mL MDV Recalled Due to Sterility Assurance Concerns

    Red Mountain Compounding Pharmacy is recalling Glutathione 200mg/mL MDV (multiple-dose vials) because FDA inspection identified concerns that the product may lack proper sterility assurance. The product was distributed to patients in multiple states.

    Product
    GLUTATHIONE 200MG/ML MDV, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Food)·F-0074-2022·2021-11-03

    Nature's Heart Mango Turmeric Cashew Mix Recalled for Undeclared Peanuts

    Nestle USA Inc. is recalling Nature's Heart Mango Turmeric Cashew Glazed Mix 1.5oz pouches due to undeclared peanut allergen. The product was distributed across 32 states.

    Product
    Nature's Heart Mango Turmeric Cashew Glazed Mix 1.5oz poly film pouches - 32 units per case
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Drugs)·D-0033-2022·2021-11-03

    Ascorbic/Glutathione Eye Solution Recalled for Sterility Concerns

    Red Mountain Compounding Pharmacy is recalling an ascorbic/glutathione eye solution because FDA inspection identified concerns about sterility assurance during manufacturing.

    Product
    ASCORBIC/GLUTATHIONE 1.25/1.25% OPTH SOLN, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0057-2022·2021-11-03

    Folic Acid 10mg/mL Injectable Recalled Due to Sterility Concerns

    Red Mountain Compounding Pharmacy is recalling folic acid injectable medication because the FDA found the product lacks adequate sterility assurance. The recall affects prescriptions distributed across multiple states.

    Product
    FOLIC ACID 10MG/ML MDV INJ, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0042-2022·2021-11-03

    Red Mountain Compounding Test Cypionate Sterility Assurance Recall

    Red Mountain Compounding Pharmacy is recalling Test Cypionate 100MG/ML in Ethyl Oleate Oil due to FDA inspection findings of sterility assurance concerns.

    Product
    TEST CYP 100MG/ML IN ETHYL OLEATE OIL, Rx only, Red Mountain Compounding Rx
    Category
    Drug
    Distribution
    7 states