The Recall Desk

State

Minnesota product recalls

73,509 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.

Which agencies issued them

These figures cover only the 7,844 recalls whose distribution notice names Minnesota specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23426–23450 of 81353

  • ModerateFDA (Food)·F-0872-2022·2022-03-23

    FDA Recalls Seasoning Product for Undeclared Wheat Allergen

    PS Seasoning & Spices, Inc. recalled Maplewood Meats Honey BBQ Stick Seasoning (lot 2022-53578) for undeclared wheat. The product was distributed across multiple U.S. states and Canada; consumers with wheat allergies should not use it.

    Product
    Maplewood Meats Honey BBQ Stick Seasoning Net Wt 21 lbs. (9.50kg). Part #180002067. Ingredients: Sugar, Salt, Dried Honey, Spices, Brown Sugar, Onion and Garlic Powder, Monosodium Glutamate, Natural Smoke Flavor, Sodium Erythorbate (0.26%), Dried Molasses, Natural Flavors…
    Category
    Food
    Distribution
    27 states
  • ModerateFDA (Drugs)·D-0653-2022·2022-03-23

    hydrALAZINE HCl Tablets 10 mg Recalled for Failed Impurity Specifications

    The Harvard Drug Group is recalling hydrALAZINE HCl Tablets, USP, 10 mg due to failed impurity and degradation specifications detected during routine stability testing. The recall affects 5,953 cartons distributed nationwide.

    Product
    hydrALAZINE HCl Tablets, USP, 10 mg, 100 Tablets per carton (10x10 blister packs), Rx only, Distributed by: MAJOR PHARMACEUTICALS, Livonia, MI 48152 USA. NDC # 0904-6440-61
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0873-2022·2022-03-23

    WAP Honey BBQ Seasoning Recalled Due to Undeclared Wheat Allergen

    PS Seasoning & Spices, Inc. is recalling WAP Honey BBQ Seasoning because it contains undeclared wheat. Consumers with wheat allergies should not consume this product.

    Product
    WAP Honey BBQ Seasoning Net Wt 20.64 lbs. (9.36kg). Part #180002073. Ingredients: Raw Cane Sugar, Sea Salt, Dried Honey, Spices, Brown Sugar, Onion and Garlic Powder, Dried Molasses, Natural Flavors.
    Category
    Food
    Distribution
    27 states
  • ModerateFDA (Devices)·Z-0802-2022·2022-03-23

    Calcium Alginate Wound Dressings Recalled for Incorrect Instructions

    CellEra LLC is recalling Vitale Silver calcium alginate wound dressings nationwide due to incorrect instructions for use containing language beyond FDA-cleared content.

    Product
    20522 Vitale Silver calcium Alginate Dressings 2x2, 10/box
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0804-2022·2022-03-23

    Calcium alginate wound dressings recalled for incorrect instruction labeling

    CellEra LLC is recalling Vitale Silver calcium alginate dressings because the included Instructions for Use contain language exceeding FDA clearance. The firm is replacing affected units with correct instructions.

    Product
    20545 Vitale Silver calcium Alginate Dressings 4x5, 10/box
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0801-2022·2022-03-23

    Medical dressing recall issued due to incorrect instructions for use

    CellEra LLC recalls Vitale Silver calcium Alginate Dressing Ropes due to incorrect Instructions for Use in product packaging. The manufacturer is replacing affected units with corrected instructions.

    Product
    20500 Vitale Silver calcium Alginate Dressing Ropes, 5/box
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0803-2022·2022-03-23

    Medical device wound dressing recall for incorrect instructions

    CellEra LLC is recalling Vitale Silver calcium Alginate Dressings because product packages contain incorrect Instructions for Use with language beyond FDA 510(k) clearance scope. The firm is replacing affected units with correct instructions.

    Product
    20544 Vitale Silver calcium Alginate Dressings 4x4, 10/box
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V172000·2022-03-22

    Marion Body Works Recalls 2018 International SR525 Emergency Vehicle

    Marion Body Works is recalling one 2018 International SR525 emergency vehicle because the engine may overcome the parking brake, increasing crash risk.

    Product
    MARION BODY WORKS — MARION BODY WORKS INTERNATIONAL SR525
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V173000·2022-03-22

    Hi-Tech E.V.S. Recalls Spartan Emergency Vehicles for Display Defect

    Hi-Tech E.V.S. is recalling 2020 Spartan MetroStar and 2021 Spartan Gladiator emergency vehicles because LCD displays may lock up, potentially delaying emergency efforts.

    Product
    HI-TECH E.V.S. — HI-TECH E.V.S. SPARTAN METROSTAR, SPARTAN GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V170000·2022-03-21

    2022 Heartland Travel Trailers Recalled for Electrical Fire Risk

    Heartland is recalling certain 2022 Trail Runner, Prowler, and Lithium travel trailers with defective power inlet bolts that may loosen, creating an electrical fire hazard. Dealers will inspect and replace the inlet free of charge.

    Product
    HEARTLAND — HEARTLAND PROWLER, LITHIUM, TRAIL RUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E023000·2022-03-19

    ZH Brothers Recalls Epicord 50-amp Shore Power Inlets Due to Fire Risk

    ZH Brothers is recalling Epicord 50-amp Shore Power Inlets because loose wiring connections may cause electrical arcs or shorts, increasing the risk of fire.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V168000·2022-03-18

    Mercedes-Benz Recalls Vehicles for Software Configuration Errors

    Mercedes-Benz is recalling specific 2007-2014 models because incorrect software updates may cause loss of drive power or control functions, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ E350, G550, SLK280, CLK550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E021000·2022-03-18

    Dometic Recalls 2-Burner Cooktops Due to Gas Leak Risk

    Dometic is recalling specific 2-burner cooktops because damaged burner control valves may cause a gas leak, increasing the risk of fire.

    Product
    EQUIPMENT:APPLIANCE:OVEN/STOVE/COOKTOP recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V167000·2022-03-18

    Mercedes-Benz Recalls S-Class and EQS Models for Turn Signal Software Error

    Mercedes-Benz is recalling 2021 S 500/S 580 and 2022 EQS 450/580 vehicles because a software error may disable rear turn signals, hazard lights, and reverse lights.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ S 500, EQS 580, EQS 450, S 580
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V169000·2022-03-18

    Tesla Recalls Model 3, S, and X for Rearview Camera Delay

    Tesla is recalling certain Model 3, S, and X vehicles because the rearview camera image may not display immediately when reversing, increasing crash risk.

    Product
    TESLA — TESLA MODEL 3, MODEL S, MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·22101·2022-03-17

    HD Premier Recalls DigitDots Magnetic Balls Due to Ingestion Hazard

    HD Premier is recalling DigitDots 3mm and 5mm magnetic balls because swallowed magnets can lodge in the digestive system, causing perforation, blockage, infection, and potentially death. Four children have required surgery to remove ingested DigitDots.

    Product
    DigitDots 3mm and 5mm Magnetic Balls
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·22734·2022-03-17

    ToolGuards Portable Water Immersion Heaters Recalled for Shock and Fire Hazards

    FXswede AB is recalling about 5,000 ToolGuards Portable Water Immersion Heaters sold on Amazon.com because the units can overheat, melt, or catch fire, creating electrocution and fire hazards. The firm has received 19 reports of overheating or fires and 2 reports of consumer shock.

    Product
    ToolGuards Portable Water Immersion Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V166000·2022-03-17

    Newmar motorhomes recalled for loose steering column bolt

    Newmar is recalling 1,277 of its 2021 and 2022 motorhomes because the steering column bolt may not be properly tightened, potentially causing loss of steering control. Owners should contact dealers for free inspection and tightening.

    Product
    NEWMAR — NEWMAR NEW AIRE, DUTCH STAR, LONDON AIRE, KOUNTRY STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V164000·2022-03-17

    International LT vehicles recalled for battery cable fire risk

    Navistar is recalling 2018-2023 International LT vehicles with 1500W Purkeys inverter systems. The positive battery cable may be incorrectly routed, causing it to chafe and become damaged, which increases the risk of electrical fire.

    Product
    INTERNATIONAL — INTERNATIONAL LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V165000·2022-03-17

    GM Recalls 2014-2015 Chevrolet Equinox and GMC Terrain for Wiper Defect

    General Motors is recalling 2014-2015 Chevrolet Equinox and GMC Terrain vehicles because corroded ball joints may cause windshield wipers to fail, reducing visibility.

    Product
    GMC — GMC, CHEVROLET TERRAIN, EQUINOX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22733·2022-03-17

    Acme United Recalls PhysiciansCare Over-the-Counter Drugs for Non-Compliant Packaging

    Acme United is recalling PhysiciansCare brand over-the-counter pain relievers and aspirin because the packaging is not child-resistant as required by law, creating a poisoning risk for young children.

    Product
    PhysiciansCare brand Aspirin, Extra Strength Non Aspirin, Extra Strength Pain Reliever, Ibuprofen, Medication Station, and Multi-Pack
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0941-2022·2022-03-16

    Abbott Similac For Spit Up Infant Formula Recalled for Cronobacter and Salmonella Contamination

    Abbott Similac For Spit Up Infant Formula with Iron is recalled due to consumer complaints of Cronobacter sakazakii and Salmonella Newport, with evidence of Cronobacter sakazakii found in the manufacturing facility.

    Product
    Abbott Similac For Spit Up Infant Formula with Iron 7oz. can and 19.5oz. plastic jar. 6 units per case. Item numbers: 67927 68086 Retail UPCs: 070074679280 070074680873
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0930-2022·2022-03-16

    Abbott Similac Pro-Sensitive Infant Formula Recalled for Cronobacter and Salmonella

    Abbott Similac Pro-Sensitive Infant Formula is being recalled due to consumer complaints of Cronobacter sakazakii and Salmonella Newport in infants, with evidence of Cronobacter found in the manufacturing facility.

    Product
    Abbott Similac Pro-Sensitive Infant Formula with Iron 20.1oz. and 22.5oz. plastic jar. 4 jars per case; 34oz. plastic jar. 6 jars per case; 7oz. can. 6 cans per case. Item numbers: 66084 66657 67923 68090 Retail UPCs: 070074660820 070074666587 070074679242…
    Category
    Food
    Distribution
    Distributed nationwide