The Recall Desk

State

Minnesota product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53901–53925 of 81678

  • ModerateFDA (Devices)·Z-2001-2016·2016-06-22

    Natus neoBLUE Phototherapy System Recall for Warning Label Update

    Natus Medical is recalling 13,541 neoBLUE Phototherapy systems to add a warning statement to the instructions and provide a laminated Quick Guide for each device.

    Product
    Natus neoBLUE Phototherapy system, Catalogue Part Number: 010066. Top Assembly Part Numbers: 001103, 001314, 002110, 040906, 040904, 040756, 040758, 040658, 040680. Product Usage: Used to provide treatment for neonatal hyperbilirubinemia
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1031-2016·2016-06-22

    Galderma Recalls Doxycycline Capsules Due to Missing Lot and Expiration Dates

    Galderma Laboratories is recalling Doxycycline USP Capsules 40 mg because some bottles are missing lot numbers or expiration dates.

    Product
    Doxycycline, USP Capsules 40 mg, Packaged in 30 ct Bottles, Rx Only. Marketed by: Prasco Laboratories, Mason, OH 45040 USA, Manufactured by: Catalent Pharma Solutions, LLC, Winchester, Kentucky 40391. NDC: 66993-815-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1034-2016·2016-06-22

    Valeant Recalls Librax Capsules Due to Failed Impurity Specifications

    Valeant Pharmaceuticals is recalling specific lots of Librax capsules because they failed impurity and degradation specifications.

    Product
    LIBRAX — LIBRAX (CHLORDIAZEPOXIDE HYDROCHLORIDE AND CLIDINIUM BROMIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1948-2016·2016-06-22

    Leica Biosystems Recalls Ariol Automated Scanning Microscopes Due to Software Issue

    Leica Biosystems Richmond Inc. is recalling 33 Ariol automated scanning microscope systems because a manufacturing error resulted in an improperly activated Windows 7 operating system.

    Product
    Ariol is an automated scanning microscope and image analysis system. It is intended for in vitro diagnostic use as an aid to the pathologist in the detection, classification, and counting of cells of interest based on particular color, intensity, size, pattern, and shape.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1036-2016·2016-06-22

    Sandoz Recalls Lisinopril Tablets Due to Missing Package Insert

    Sandoz Inc is recalling 3,048 bottles of Lisinopril Tablets USP, 30 mg, because the package insert is incorrect or missing.

    Product
    Lisinopril Tablets USP, 30 mg, 100-count bottle, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08540, NDC 0185-0630-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V450000·2016-06-21

    Forest River Recalls 2016-2017 Flagstaff and Work N' Play Trailers

    Forest River is recalling 2016-2017 Flagstaff and Work N' Play trailers because a propane regulator sight glass may crack, allowing gas to leak and potentially cause a fire.

    Product
    FOREST RIVER — FOREST RIVER FLAGSTAFF, WORK AND PLAY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V452000·2016-06-21

    Navistar Recalls 2016 IC Bus RE School Buses for Seat Defect

    Navistar is recalling 2016 IC Bus RE school buses because child seats may separate from the base frame due to bolt failure, increasing injury risk in a crash.

    Product
    IC BUS — IC BUS RESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16199·2016-06-21

    Tommee Tippee Electric Bottle and Food Warmers Recalled for Fire Hazard

    Mayborn USA is recalling about 255,000 Tommee Tippee electric bottle and food warmers due to a fire hazard. The units can overheat, melt, smoke, and catch fire.

    Product
    Electric bottle and food warmers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V449000·2016-06-21

    GM Recalls 2016 Chevrolet Equinox and GMC Terrain for Incorrect Tire Labels

    General Motors is recalling specific 2016 Chevrolet Equinox and GMC Terrain vehicles because their certification labels may display incorrect tire and rim size information.

    Product
    GMC — GMC, CHEVROLET TERRAIN, EQUINOX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V451000·2016-06-21

    Gillig Recalls 2012-2016 Low Floor Vehicles Due to Flashing Brake Lights

    Gillig is recalling 112 model year 2012-2016 Low Floor vehicles because the rear brake lights may flash inadvertently, which could confuse other drivers and increase crash risk.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V453000·2016-06-21

    Navistar Recalls 2017 International Trucks Due to Engine Stall Risk

    Navistar is recalling 1,191 model year 2017 International trucks because an electrical short in the engine control module can cause the engine to stall without restarting.

    Product
    INTERNATIONAL — INTERNATIONAL LONESTAR, PROSTAR, PAYSTAR, HX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V447000·2016-06-20

    Eldorado Shuttle Buses Recalled for Electrical Component Fire Risk

    Eldorado is recalling 2016 Aerotech, Aero Elite, and Advantage shuttle buses because a component in the electrical power distribution center may break, causing electrical arcing and increasing the risk of fire.

    Product
    ELDORADO — ELDORADO ADVANTAGE, AEROTECH, AERO ELITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E058000·2016-06-20

    Speedtech Recalls Nitrous Solenoid Valves Due to Welding Defect

    Speedtech LLC is recalling Nitrous Solenoid Valves used in drag racing nitrous oxide systems because improper welding may cause the valve to separate and eject the piston under pressure.

    Product
    FUEL SYSTEM, OTHER:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·051-2016·2016-06-18

    GNP Company Recalls Chicken Products Due To Foreign Matter Contamination

    GNP Company is recalling approximately 55,608 pounds of chicken products that may be contaminated with sand and black soil. No illnesses have been reported.

    Product
    Pilgrim's Pride Corporation — GNP Company Recalls Chicken Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16V446000·2016-06-17

    Indian Recalls 2014-2016 Motorcycles Due to Fire Risk

    Indian Motorcycle is recalling 2014-2016 models because engine misfires can raise exhaust temperatures, increasing the risk of fire.

    Product
    INDIAN — INDIAN CHIEF CLASSIC, CHIEFTAIN, ROADMASTER, VINTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V441000·2016-06-16

    Eldorado Amerivan 10 Recall for Fuel Line Leak Fire Risk

    Eldorado is recalling 2012-2016 Amerivan 10 vehicles because an improperly installed fuel line may leak and cause a fire.

    Product
    ELDORADO — ELDORADO AMERIVAN 10
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V442000·2016-06-16

    Mercedes-Benz Recalls 2015-2016 Models for Seatbelt Anchor Bolt Defect

    Mercedes-Benz is recalling certain 2015-2016 models because the right rear seatbelt anchor bolt may be incorrectly installed, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE450, AMG ML63, ML250, ML350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V443000·2016-06-16

    E-One Recalls Cyclone II and Typhoon Vehicles for Electrical Fire Risk

    E-One is recalling 2014-2016 Cyclone II and Typhoon vehicles because a power control module defect may cause a short circuit, leading to electrical damage or fire.

    Product
    E-ONE — E-ONE CYCLONE II, TYPHOON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V444000·2016-06-16

    Land Rover Recalls 2016 LR4 Vehicles Due to Frontal Air Bag Defect

    Jaguar Land Rover is recalling 2016 LR4 vehicles because the driver-side frontal air bag may not inflate properly, increasing injury risk in a crash.

    Product
    LAND ROVER — LAND ROVER LR4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0966-2016·2016-06-15

    FDA Recalls Thin and Slim Thermogenic Fat Burner for Unapproved Ingredient

    Novacare, LLC is recalling The Store Thin and Slim Thermogenic Fat Burner because FDA sampling found salicylic acid, an ingredient not approved for dietary supplements.

    Product
    The Store Thin and Slim Thermogenic Fat Burner Dietary Supplement packaged in 90 capsule containers. Distributed by The Store 2050 E. 6200 S., Holladay, UT 84121, The Store Holliday, 4695 S.Holladay Blvd, Holladay, UT 84117, The Store Midway, 42 W. Main Street, Midway, UT 84049.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0964-2016·2016-06-15

    Novacare Recalls MetaPro 360 Supplement Containing Unapproved Salicylic Acid

    Novacare, LLC is recalling MetaPro 360 Metabolic Accelerator dietary supplements because FDA sampling confirmed the presence of salicylic acid, an unapproved drug ingredient.

    Product
    MetaPro 360 Metabolic Accelerator Dietary Supplement packaged in 120 capsule containers. www.metapro360.com 877-778-7509.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0970-2016·2016-06-15

    FDA Recalls Asia Black 25 Ephedra Extreme Fat Burner for Unapproved Ingredients

    Novacare, LLC is recalling Asia Black 25 Ephedra Extreme Fat Burner because FDA sampling confirmed the presence of salicylic acid, an unapproved ingredient in dietary supplements.

    Product
    Asia Black 25 Ephedra Extreme Fat Burner Potent Dietary Supplement packaged in 100 capsule containers. Distributed by Cloma Pharma Laboratories, Samford, CT 06902.
    Category
    Drug
    Distribution
    Distributed nationwide