The Recall Desk

State

Minnesota product recalls

73,737 recalls have nationwide distribution and so reach Minnesota. 7,849 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total
7,849
Critical
1,137
Severe
2,245
Most recent
2026-10-28

Of the 7,849 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 2,245 (29%) are Severe.

These figures cover only the 7,849 recalls whose distribution notice names Minnesota specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32851–32875 of 81586

  • ModerateFDA (Devices)·Z-1366-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they may cause incorrect rotation and margin misalignment in dental impressions.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 3.8MM(P) X 3MM(H) Reference Number: IEHA343
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0780-2020·2020-03-04

    Nature's Sunshine CMapt M SmartMeal Recalled for Unapproved Herbicide in Flax Seed

    Pro-Form Manufacturing LLC is recalling Nature's Sunshine CMapt M SmartMeal products because the flax seed used contains an unapproved herbicide.

    Product
    Nature's Sunshine CMapt M - Cmapt Mi- SmartMeal; Bahu bhbhi - Vanilla; 510 g UPC: 0 99904 03085 5 Product number: 6116-RU3085 6116-UA3085 Distributed in Russia and Ukraine - same label Nature's Sunshine Products Inc. 2500 West Executive…
    Category
    Food
    Distribution
    2 states
  • LowFDA (Drugs)·D-0859-2020·2020-03-04

    Akorn Recalls Sodium Chloride Ophthalmic Ointment Due to Particulate Matter

    Akorn, Inc. is recalling specific lots of Sodium Chloride Ophthalmic Ointment USP, 5%, due to the presence of brown particulate matter inside the tubes.

    Product
    Sodium Chloride Ophthalmic Ointment USP, 5%, 3.5 g tubes, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC 17478-622-35
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1389-2020·2020-03-04

    LivaNova SMART PERFUSION PACK INSPIRE 8S Recalled for Incorrect Cuvette Packaging

    LivaNova USA Inc. is recalling 27 SMART PERFUSION PACK INSPIRE 8S units because they were packaged with the incorrect cuvette component.

    Product
    LivaNova SMART PERFUSION PACK INSPIRE 8S - Product Usage: The affected product is a perfusion tubing pack use in surgical procedures requiring extracorporeal support. The perfusion tubing packs include the cuvette used with equipment to monitor blood.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1063-2020·2020-03-04

    Breckenridge Recalls Zoledronic Acid Injection Due to Impurity Failures

    Breckenridge Pharmaceutical is recalling 900 vials of Zoledronic Acid Injection because stability testing revealed out-of-specification impurities.

    Product
    Zoledronic Acid Injection 5 mg/100 mL (0.05 mg/mL), Solution for Intravenous Infusion, Sterile Solution, 100 mL Single - Dose Vial per Carton, Rx Only, Distributed by: Breckenridge Pharmaceutical, Inc., Boca Raton, FL 33487, Manufactured by: Pharmaceutics International, Inc.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0781-2020·2020-03-04

    Nature's Sunshine NutriSmart Soy Powder Recalled for Unapproved Herbicide

    Pro-Form Manufacturing LLC is recalling Nature's Sunshine NutriSmart soy protein powder because the flax seed ingredient contains an unapproved herbicide.

    Product
    Nature's Sunshine NutriSmart Mezcla en polvo a base de proteina de soya enriquecida con vitaminas y minerals; Vainilla Plastic HDPE jar Contenido Neto 510 g UPC: 0 80030910217 Product number: 6116-GE3091 Elaborado por: Nature's Sunshine Products Inc. 1655 North Main…
    Category
    Food
    Distribution
    2 states
  • LowFDA (Devices)·Z-1391-2020·2020-03-04

    Getinge 46-Series Washer Disinfector Recalled Due to Missing Water Intake

    Maquet Cardiovascular is recalling 7 Getinge 46-Series Washer Disinfector units because they lack the necessary water intake components for proper installation.

    Product
    Getinge 46-Series Washer Disinfector Model # 46-4, Part Number:46-4-503 Product Usage: Used in facilities such as Central Sterile Supply Departments, next to the Operating Room, in dental clinics or hospital wards to clean, thermally or chemically disinfect and dry surgical…
    Category
    Medical Device
    Distribution
    7 states
  • LowFDA (Devices)·Z-1390-2020·2020-03-04

    Getinge 46-Series Washer Disinfector Recalled Due to Missing Water Intake Components

    Maquet Cardiovascular is recalling four Getinge 46-Series Washer Disinfector units because they lack necessary water intake components, preventing proper installation.

    Product
    Getinge 46-Series Washer Disinfector Model # 46-4, Part Number:46-4-502 Product Usage: Used in facilities such as Central Sterile Supply Departments, next to the Operating Room, in dental clinics or hospital wards to clean, thermally or chemically disinfect and dry surgical…
    Category
    Medical Device
    Distribution
    7 states
  • LowFDA (Drugs)·D-0856-2020·2020-03-04

    Golden State Medical Supply Recalls Tramadol Tablets Due to Labeling Error

    Golden State Medical Supply is recalling Tramadol Hydrochloride 50 mg tablets because the patient leaflets contain incorrect dosing instructions for unscored tablets.

    Product
    TRAMADOL HYDROCHLORIDE Tablets, USP, 50 mg, Rx Only a)100-count bottles (NDC 60429-588-01) b) 500-count bottle (NDC 60429-588-05) Manufactured by Teva Czech Industries, s.r.o. Opava-Komarov, Czech Republic, Packaged by GSMS Incorporated, Camarillo, CA 93012
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0860-2020·2020-03-04

    Akorn Recalls Well at Walgreens Sodium Chloride Ophthalmic Ointment Due to Particulate Matter

    Akorn, Inc. is recalling specific tubes of Well at Walgreens Sodium Chloride Ophthalmic Ointment USP, 5%, due to the presence of brown spots identified as tin with trace copper.

    Product
    Well at Walgreens Sodium Chloride Ophthalmic Ointment USP, 5%, 3.5 g tubes, Distributed by: Walgreen Co. 200 Wilmot Rd., Deerfield, IL 60015. NDC 0363-9050-00.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0861-2020·2020-03-04

    CVS Health Sodium Chloride Ophthalmic Ointment Recalled for Particulate Matter

    Akorn, Inc. is recalling CVS Health Sodium Chloride Ophthalmic Ointment USP, 5%, due to the presence of brown spots identified as tin with trace copper inside the tubes.

    Product
    CVS Health Sodium Chloride Ophthalmic Ointment USP, 5%, 3.5 g tubes, Distributed By: CVS Pharmacy Inc. One CVS Drive, Woonsocket, RI 02895, NDC 59779-303-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V126000·2020-03-03

    Thomas Built Buses Recall 2019-2020 Models for Brake Caliper Bolt Issue

    Daimler Trucks is recalling 581 Thomas Built school buses because loose brake caliper bolts may reduce braking effectiveness, increasing crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2, SAF-T-LINER HDX, SAF-T-LINER EFX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V125000·2020-03-03

    Blue Bird Recalls School Buses Due to Seat Barrier Defect

    Blue Bird is recalling 2008-2021 Vision and All American school buses because the seat barrier behind the driver may be missing a reinforcing bracket, increasing injury risk in a crash.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION SCHOOL BUS, VISION TRANSIT BUS, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V127000·2020-03-03

    Daimler Trucks Recalls 2019-2020 Vehicles for Brake Caliper Bolt Issue

    Daimler Trucks North America is recalling 2,585 2019-2020 trucks because brake caliper mounting bolts may be loose, increasing crash risk.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER, FCCC 4700, 5700, BUSINESS CLASS M2, XBR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V124000·2020-03-03

    Jeep Recalls Wrangler and Gladiator Vehicles for Clutch Fire Risk

    Chrysler is recalling 2018-2020 Jeep Wrangler and 2020 Gladiator vehicles with manual transmissions because the clutch pressure plate may overheat and fracture, increasing the risk of fire or crash.

    Product
    JEEP — JEEP WRANGLER, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20T005000·2020-03-03

    Tires Recalled for Sidewall Separation Defect

    Sentury Tire is recalling certain sidewall-tired models because a manufacturing defect causes the sidewall to separate, potentially leading to tire failure and increased crash risk.

    Product
    TIRES:SIDEWALL recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V121000·2020-02-28

    Hyundai Recalls 2013-2014 Sonata Vehicles for Fuel Hose Fire Risk

    Hyundai is recalling 2013-2014 Sonata vehicles because a fuel hose may crack, causing a leak and increasing fire risk. Dealers will inspect and repair the hose free of charge.

    Product
    HYUNDAI — HYUNDAI SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V120000·2020-02-28

    Pierce Emergency Fire Vehicles Recalled for Aerial Device Cracks

    Pierce is recalling 2019-2020 Arrow XT, Enforcer, Impel, and Velocity fire vehicles because cracks in the aerial device tube may cause it to fall.

    Product
    PIERCE — PIERCE ARROW XT, IMPEL, VELOCITY, ENFORCER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V122000·2020-02-28

    Hyundai Recalls 2020 Sonata Vehicles for Incorrect Tire Size Labeling

    Hyundai is recalling 2020 Sonata vehicles because the tire pressure label and owner's manual list an incorrect tire size. This error may lead owners to install the wrong tires, affecting vehicle handling.

    Product
    HYUNDAI — HYUNDAI SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V119000·2020-02-28

    Forest River Shasta Trailers Recalled for Tire Clearance Issues

    Forest River is recalling 2020 Shasta SST240TH and SST260TH trailers because tires may contact the wheel well, risking tire failure and loss of control.

    Product
    FOREST RIVER — FOREST RIVER SHASTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20083·2020-02-27

    Lennox Recalls Ductless Heat Pumps Due to Fire Hazard

    Lennox is recalling about 1,650 ductless heat pumps sold in the U.S. because internal electrical components can fail and overheat, posing a fire hazard.

    Product
    Lennox Ductless Single-Zone and Multi-Zone heat pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V115000·2020-02-27

    Altec Recalls 2019 Aerial Devices Due to Fastener Failure Risk

    Altec Industries is recalling 238 specific 2019 aerial devices because high-strength fasteners securing the pedestal to the turntable may fail, potentially causing the pedestal to separate.

    Product
    ALTEC — ALTEC LR756, TDA58, L42M, LR760
    Category
    Vehicle
    Distribution
    Distributed nationwide