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.

45251–45275 of 81660

  • ModerateFDA (Devices)·Z-0080-2018·2017-11-15

    Boston Scientific Recalls Four Momentum X4 CRT-D Devices for Firmware Error

    Boston Scientific is recalling four Momentum X4 CRT-D devices due to incorrect firmware configuration. The devices were distributed to medical facilities in Minnesota and Ohio.

    Product
    MOMENTUM X4 CRT-D, Model G138, Sterile.
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0066-2018·2017-11-15

    Encore Medical Recalls Cobalt Bone Cement Due to Packaging Seal Loss

    Encore Medical, Lp is recalling 1,815 units of Cobalt MV with Gentamicin bone cement because the sterile Tyvek packaging seal was lost.

    Product
    Cobalt MV with Gentamicin, Cobalt Bone Cement 40GM, REF 402439, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0077-2018·2017-11-15

    Boston Scientific Recalls Five Resonate EL ICD VR Devices for Firmware Error

    Boston Scientific is recalling five Resonate EL ICD VR devices due to incorrect firmware configuration. The devices were distributed to medical facilities in Minnesota and Ohio.

    Product
    RESONATE EL ICD VR, Model D432, Sterile.
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0064-2018·2017-11-15

    Biomet Cobalt HV Bone Cement Recalled for Packaging Seal Loss

    Encore Medical is recalling Biomet Cobalt HV Bone Cement because the sterile Tyvek packaging seal may be lost, potentially compromising sterility.

    Product
    Cobalt HV Bone Cement 40GM, REF 402282, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic parts to living bone when…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0079-2018·2017-11-15

    Boston Scientific Recalls Four VIGILANT X4 CRT-D Devices for Firmware Error

    Boston Scientific is recalling four VIGILANT X4 CRT-D devices due to incorrect firmware configuration. The devices were distributed to medical facilities in Minnesota and Ohio.

    Product
    VIGILANT X4 CRT-D, Model G247, Sterile. Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) are indicated for patients with heart failure who receive stable optimal pharmacologic therapy (OPT) for heart failure and who meet any one of the following classifications…
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0071-2018·2017-11-15

    Aaren Scientific AERO IOL Injection System Recalled for Incorrect Storage Labeling

    Aaren Scientific Inc. is recalling 786 boxes of AERO IOL Injection Systems because the recommended storage temperature on the label is incorrect.

    Product
    AERO IOL Injection System containing 10 Z28 Cartridges per box, Part #003500-0025-282, Sterile, Rx. The firm name on the label is Aaren Scientific Inc., Ontario, CA. Used to fold and insert the firm's IOL's.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0349-2018·2017-11-15

    Harmless Harvest Recalls Probiotic Drinks Due to Premature Spoilage

    Harmless Harvest is recalling four varieties of probiotic drinks because testing identified Candida lusitaniae as the cause of premature spoilage.

    Product
    Harmless Coconut Probiotics Original; Coconut Cultured Beverage; UPC 859078-002542; Keep refrigerated 11 lf. oz. HDPE Bottle Ingredients: Organic Coconut Water, Water, Organic Coconut Meat, Organic Cane Sugar, live and active cultures. Harmless Harvest
    Category
    Food
    Distribution
    5 states
  • LowFDA (Drugs)·D-0072-2018·2017-11-15

    Doan's Pain Relieving Cream Recalled for Packaging Labeling Mismatch

    Dr. Reddy's is recalling Doan's Pain Relieving Cream because the lot number on the outer packaging does not match the bottle. This is a Class III labeling recall.

    Product
    Doan's Pain Relieving Cream with 4% Lidocaine Plus Menthol, (lidocaine 4%, menthol 1%), Net Wt. 2.75 oz. (77.3 g) Tube, Distributed by: Ducere Pharma, LLC New Hope, PA 18938 USA --- UPC 849648000023
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V714000·2017-11-14

    Mercedes-Benz Recalls 2017 Models for Power Steering Overheating Risk

    Mercedes-Benz is recalling 72 vehicles from 2017 models due to a power steering control unit defect that may disable assist, increasing crash risk.

    Product
    MERCEDES-MAYBACH — MERCEDES-MAYBACH, MERCEDES-BENZ S600, S65 AMG, E300, S550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V713000·2017-11-14

    Mercedes-Benz Recalls 2016-2017 G-Class Vehicles for ESP Malfunction

    Mercedes-Benz is recalling 2016-2017 G550, G63, and G65 vehicles because an ESP malfunction may prevent the engine from reducing power, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG G65, G63, G550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·18028·2017-11-14

    Go Wheels Hoverboards Recalled Due to Fire and Explosion Hazards

    Four Star Imports is recalling Go Wheels self-balancing scooters sold at Village Mart because the lithium-ion batteries can overheat, posing fire and explosion risks.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V726000·2017-11-14

    Isuzu and Chevrolet Trucks Recall Defective Fire Extinguishers

    Isuzu is recalling certain 2008-2018 Isuzu and Chevrolet trucks because the installed fire extinguishers may clog, require excessive force to activate, or detach, posing injury risks.

    Product
    ISUZU — ISUZU, CHEVROLET NRR, NQR, NPR XD, NPR HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18029·2017-11-14

    Simplified Wireless Recalls iHoverspeed Hoverboards Due to Fire Hazard

    Simplified Wireless is recalling about 900 iHoverspeed self-balancing scooters because their lithium-ion batteries can overheat, posing a risk of fire or explosion.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V712000·2017-11-14

    Ram ProMaster Recall: Incorrect Rivet May Affect Side Airbag Deployment

    Chrysler is recalling 2018 Ram ProMaster vehicles because an incorrect rivet may cause the front door impact sensor to fracture, potentially affecting side airbag deployment.

    Product
    RAM — RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V715000·2017-11-14

    Mercedes-Benz Recalls GLC Models for Sunroof Panel Bonding Defect

    Mercedes-Benz is recalling 2017-2018 GLC300 and GLC43 AMG vehicles because sunroof panels may separate, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC300, AMG GLC43, GLC 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·17V711000·2017-11-14

    Forest River Recalls 2018 Prime Time Fury Trailers for Incorrect Placards

    Forest River is recalling 2018 Prime Time Fury recreational trailers because the Federal Placard lists incorrect tire and rim sizes, which could lead to the installation of wrong replacement tires.

    Product
    PRIME TIME — PRIME TIME FURY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V709000·2017-11-13

    Altec Recalls Aerial Cable Placers Due to Boom Tip Crack Risk

    Altec Industries is recalling 1992-2000 Aerial Cable Placer AP45 vehicles because boom tips may crack and fail, increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL CABLE PLACER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E067000·2017-11-13

    IMT Recalls Dominator I Crane Bodies Due to Stabilizer Pin Defect

    Iowa Mold Tooling Co. is recalling Dominator I crane bodies because incorrect stabilizer arm locking pins may fail to engage, allowing the arm to extend while driving.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V710000·2017-11-13

    Pleasant Valley Recalls Travel Trailers Due to Fire Extinguisher Defect

    Pleasant Valley is recalling 2017-2018 travel trailers and truck campers because the installed fire extinguishers may clog or detach, potentially failing to work during a fire.

    Product
    PLEASANT VALLEY — PLEASANT VALLEY MYPOD TRAVEL TRAILER, CIRRUS TRUCK CAMPER, T@G TRAVEL TRAILER, T@B TRAVEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide