The Recall Desk

State

Minnesota product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

56751–56775 of 81684

  • ModerateFDA (Drugs)·D-0388-2016·2015-12-09

    Nephron Recalls Asthmanefrin Inhalation Solution Due to Discoloration

    Nephron Pharmaceuticals is voluntarily recalling Asthmanefrin inhalation solution starter kits due to discoloration. The recall covers 47,754 cartons distributed nationwide.

    Product
    Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator, Starter Kit (Racepinephrine 11.25 mg) 10 individual foil wrapped vials with 1 EZ Breathe Atomizer per carton, Manufactured By: nephron pharmaceuticals corporation, Orlando, FL --- NDC 0487-2784-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0485-2016·2015-12-09

    Northwind Pharmaceuticals Recalls Prednisone Tablets Due to Incorrect NDC Labeling

    Northwind Pharmaceuticals is recalling 40 bottles of Prednisone 20 mg tablets because the NDC number on the container is incorrect.

    Product
    Prednisone 20 mg, Tablet, 10-count bottle, Rx only, Mfg by: HIKMA Pharmaceuticals PO BOX 182400 Amman 11118 Jordan. Dist By: West-Ward Pharmaceuticals Corp., Eatentown, NJ 07724 USA, Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46256. NDC 51655-320-53
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·16710·2015-12-08

    Kubota Recalls Utility Vehicles Due to Fire Hazard

    Kubota is recalling approximately 11,500 RTV-X1100C utility vehicles because combustible debris can contact the exhaust manifold and ignite, posing a fire hazard.

    Product
    Utility Vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V823000·2015-12-08

    Audi Recalls A6 and A7 Vehicles Due to Passenger Air Bag Defect

    Volkswagen Group of America is recalling 2012-2013 Audi A6 and A7 vehicles because the passenger air bag system may fail to deploy in a crash.

    Product
    AUDI — AUDI A7, A6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16054·2015-12-08

    TCP and Great Value LED Lamps Recalled for Electrical Shock Hazard

    Technical Consumer Products is recalling specific 14-watt LED PAR38 lamps sold at Walmart and electrical distributors due to a risk of electric shock in wet locations.

    Product
    Technical Consumer Products (TCP) and Great Value LED lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V824000·2015-12-08

    Audi Recalls 2015 A3 Cabriolet for Seat Cover Stitching Defect

    Volkswagen is recalling 904 2015 Audi A3 Cabriolets because incorrectly stitched seat covers may prevent side air bags from deploying properly in a crash.

    Product
    AUDI — AUDI A3 CABRIOLET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V820000·2015-12-07

    Polaris Recalls 2015 GEM Electric Vehicles for Seat Belt Defect

    Polaris is recalling 2015 GEM electric vehicles because seat belt retractors may fail, preventing proper occupant restraint in a crash.

    Product
    GEM — GEM E6S, E4, ELXD, EL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V816000·2015-12-07

    Freightliner Cascadia CNG Vehicles Recalled for Exhaust Fire Risk

    Daimler Trucks North America is recalling 2013-2015 Freightliner Cascadia CNG vehicles because hot exhaust near the pressure relief device may cause gas release and fire.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V821000·2015-12-07

    Honda Recalls VFR1200F Motorcycles for Driveshaft Universal Joint Wear

    Honda is recalling 2010, 2012, and 2013 VFR1200F motorcycles because driveshaft universal joint bearings may wear prematurely, potentially causing the joint to separate or break.

    Product
    HONDA — HONDA VFR1200F
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V819000·2015-12-07

    Tiny Idahomes Recalls RVs With Overheating Water Heater Valves

    Tiny Idahomes is recalling 2014-2016 RVs equipped with specific Atwood water heaters that may overheat water, posing a scalding risk.

    Product
    TINY IDAHOMES — TINY IDAHOMES CASCADE, CLEAR CREEK, CARPATHIAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V814000·2015-12-03

    ShowHauler Recalls One 2013 Motorhome Due to Water Heater Overheating

    ShowHauler Trucks is recalling one 2013 ShowHauler motorhome because a defective water heater valve may cause water to overheat, posing a scalding risk.

    Product
    SHOWHAULER — SHOWHAULER MOTORHOME
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0265-2016·2015-12-02

    TN Juice Bar Recalls Refine 3-Day Cleanse Juice Kit Nationwide

    TN Juice Bar is recalling 137 units of the Refine 3-Day Cleanse juice kit nationwide due to unpasteurized juice with elevated pH levels and unlabeled almond milk.

    Product
    Refine 3-Day Cleanse, a juice kit that contains Lean Green, 16 oz (6 bottles), Beet It, 16 oz (6 bottles), Almond Milk, 8 oz (3 bottles) and Wheat grass juice, 8 oz (2 bottles)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V812000·2015-12-02

    Ford Recalls 2013 Vehicles for Fuel Delivery Module Fire Risk

    Ford is recalling 2013 Explorer, Taurus, Flex, Lincoln MKS, and MKT vehicles because a cracked fuel delivery module may leak fuel and cause a fire.

    Product
    FORD — FORD, LINCOLN TAURUS, MKT, FLEX, MKS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0327-2016·2015-12-02

    NxStage System One S Cycler Recalled for Ultrafiltration Software Error

    NxStage Medical is recalling 16 System One S Cycler units due to a software error causing inaccurate fluid removal.

    Product
    NxStage System One S Cycler (High Permeability Hemodialysis System) Model no. NX1000-5-A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0331-2016·2015-12-02

    Palindrome Precision Chronic Catheter Kit Recalled for Packaging Defect

    Covidien LLC is recalling 365 units of Palindrome Precision Chronic Catheter Kits because they were incorrectly packaged with a 90-degree bend at the distal tip.

    Product
    Palindrome Precision Chronic Catheter Kit Symmetrical Tip, Tal VenaTrac" Stylet 14.5 Fr/Ch (4.8mm) X 33 cm Item Number: 8888145042P The Palindrome chronic catheter is intended for acute and chronic hemodialysis, apheresis, and infusion. It may be inserted either…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0340-2016·2015-12-02

    Siemens ADVIA Chemistry Hemoglobin A1c Reagent Kits Recalled for Bias

    Siemens Healthcare Diagnostics is recalling specific lots of ADVIA Chemistry Hemoglobin A1c reagent kits due to a positive bias that may result in inaccurate test results.

    Product
    ADVIA Chemistry Hemoglobin A1c_3, A1c_3M Reagent kits. Used on the ADVIA 1200, 1650, 1800, 2400, and XPT Chemistry Systems. For in vitro diagnostic use in the quantitative determination of Hemoglobin A1c, a diabetes marker, in whole blood on the ADVIA Chemistry systems.
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Drugs)·D-0386-2016·2015-12-02

    Qualgen Recalls Estradiol Pellets Due to Sterility Assurance Concerns

    Qualgen is recalling 4,221 vials of compounded Estradiol USP pellets nationwide because deficient practices may have impacted sterility assurance.

    Product
    Estradiol USP 99.5%, .5% Stearic Acid NF Pellets, 3 mL, one-count vials, 6 mg (NDC 69761-006-01),10 mg (NDC 69761-010-01),12.5 mg (NDC 69761-012-01), 15 mg (NDC 69761-015-01),18 mg (NDC 69761-018-01),20 mg (NDC 69761-020-01), 22 mg (NDC 69761-022-01), 25 mg (NDC 69761-025-01)…
    Category
    Drug
    Distribution
    Distributed nationwide