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.

56476–56500 of 81684

  • HighFDA (Devices)·Z-0431-2016·2015-12-23

    bioMerieux MYLA CLI Software Recalled for Patient Data Linking Errors

    bioMerieux is recalling MYLA CLI software versions 3.x to 4.1 because it may link test results to incorrect patient records.

    Product
    MYLA CLI V3.X TO V4.1 ML350 SERVER Product Usage: MYLA is a computer application (Middleware) based on Web 2.0 technology which: Interfaces between the instruments connected to the application and the LIS(s) (Laboratory Information System(s)).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0421-2016·2015-12-23

    Verathon GlideScope AVL Video Laryngoscope Blades Recalled for Separation Risk

    Verathon is recalling GlideScope AVL video laryngoscope blades because silicone adhesive bonding may be inadequate, creating a risk of blade separation during use.

    Product
    GlideScope AVL Video Laryngoscope (AVL), Part Number AVL 3- 0574-0115; AVL 4-0574-0116, AVL 5- 0574-0117. AVL is a video laryngoscope that incorporates a high resolution color camera, an LED light source and video output to a remote monitor. This system has a digital…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0418-2016·2015-12-23

    Fujifilm Medical Systems Recalls Duodenoscopes for Reprocessing Design Changes

    Fujifilm Medical Systems is recalling specific duodenoscope models as a precautionary measure because the devices have been redesigned to incorporate a closed elevator wire channel that facilitates reprocessing.

    Product
    Fujifilm Medical Systems Duodenoscope, Model Numbers ED-200XU, ED-200XT, ED-250XT, ED-310XU, ED-420XL, ED-410XT, ED-410XU, ED-450XL, and ED-450XT. Medical endoscope for the duodenum and upper G.I. tract. Open elevator wire channel duodenoscopes.
    Category
    Medical Device
    Distribution
    13 states
  • ModerateFDA (Devices)·Z-0405-2016·2015-12-23

    Philips Brilliance 64 CT System Software Error Recall

    Philips is recalling seven Brilliance 64 CT systems because software may set the scan length differently than planned.

    Product
    Philips Healthcare Brilliance 64 Computed Tomography X-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0432-2016·2015-12-23

    Beckman Coulter Recalls DxH 800 and 600 Hematology Analyzer Software

    Beckman Coulter is recalling specific software versions for its DxH 800 and DxH 600 hematology analyzers because the software allows the creation of multiple orders with the same specimen ID but different patient IDs.

    Product
    UniCel DxH 800 Coulter Cellular Analysis System, Software Version 3.0.2.0, Part No. 629029, B24465, B24802 The UniCel DxH 800/DxH 600 analyzers are quantitative, multi-parameter, automated hematology analyzers for in vitro diagnostic use in screening patient populations found…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0433-2016·2015-12-23

    Beckman Coulter Recalls DxH 800 and DxH 600 Software Versions

    Beckman Coulter is recalling specific software versions for its DxH 800 and DxH 600 hematology analyzers because the systems allow multiple orders to share the same specimen ID with different patient IDs.

    Product
    UniCel DxH 600 Coulter Cellular Analysis System, Software Version 3.0.2.0, Part No. 775222 The UniCel DxH 800/DxH 600 analyzers are quantitative, multi-parameter, automated hematology analyzers for in vitro diagnostic use in screening patient populations found in clinical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0521-2016·2015-12-23

    Teva Recalls Irbesartan and Hydrochlorothiazide Tablets Due to Labeling Errors

    Teva Pharmaceutical Industries is recalling 3,536 bottles of Irbesartan and Hydrochlorothiazide tablets because some bottles have incorrect or missing lot and expiration dates.

    Product
    IRBESARTAN AND HYDROCHLOROTHIAZIDE — IRBESARTAN AND HYDROCHLOROTHIAZIDE (IRBESARTAN AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V864000·2015-12-22

    Hyundai Recalls 2015 Genesis Vehicles for Tire Sidewall Cracks

    Hyundai is recalling 2015 Genesis vehicles because original equipment tires may develop sidewall cracks, leading to air loss and potential loss of vehicle control.

    Product
    HYUNDAI — HYUNDAI GENESIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V862000·2015-12-22

    MCI Recalls 2016 J4500 Motor Coaches Due to Seat Mounting Defect

    Motor Coach Industries is recalling 2016 MCI J4500 motor coaches because a seat mounting bolt may be installed incorrectly, increasing injury risk in a crash.

    Product
    MCI — MCI J4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V859000·2015-12-22

    Daimler Trucks Recalls 2015-2016 Freightliner and Western Star Models for Axle Defect

    Daimler Trucks is recalling 2015-2016 Freightliner and Western Star trucks because improperly tightened axle nuts could cause the driveshaft to disconnect, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR 108SD, 4900, 114SD, BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V867000·2015-12-22

    Ford Recalls 2015 F-150 Trucks Due to Seat Belt Anchor Defect

    Ford is recalling 2015 F-150 SuperCrew trucks because improperly crimped seat belt pretensioner cables may prevent proper occupant restraint in a crash.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V863000·2015-12-22

    Kaufman Flatbed and Wedge Car Hauler Trailers Recalled for Axle Defect

    Kaufman is recalling 2016 Flatbed and Wedge Car Hauler trailers due to mismatched axle components that may cause wheel bearing failure and increase crash risk.

    Product
    KAUFMAN — KAUFMAN FLATBED, WEDGE CAR HAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V868000·2015-12-22

    Navistar Recalls School Buses with Defective Wheelchair Lifts

    Navistar is recalling certain 2007-2015 IC school buses equipped with specific Ricon wheelchair lifts. The lifts may have oversized pivot holes that allow bearings to shift, risking platform failure.

    Product
    IC BUS — IC BUS CASB, FE, RE, ICCB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16066·2015-12-22

    Breville Recalls Pressure Cookers Due to Risk of Burns

    Breville is recalling about 35,600 Fast Slow Cookers because an incorrectly inserted gasket can cause pressure release and burns.

    Product
    Breville Fast Slow Cookers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V866000·2015-12-22

    Winnebago and Itasca Motorhomes Recalled for Step Deployment Defect

    Winnebago is recalling 2015-2016 Sightseer, Vista, Adventurer, Sunova, Sunstar, and Suncruiser motorhomes because electric steps may extend while driving, increasing crash risk.

    Product
    ITASCA — ITASCA, WINNEBAGO SUNOVA, VISTA, SIGHTSEER, ADVENTURER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16717·2015-12-22

    John Deere Recalls Zero-Turn Lawn Mowers Due to Fire Risk

    John Deere is recalling about 150 zero-turn lawn mowers because a fuel hose could have been cut during manufacturing, posing a fire hazard.

    Product
    John Deere zero-turn lawn mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V858000·2015-12-22

    Ford Recalls 2016 F-650 and F-750 Trucks for Rear Brake Hose Chafing

    Ford is recalling 302 model year 2016 F-650 and F-750 trucks because rear brake hoses may chafe on the axle, potentially causing air leaks and reduced braking ability.

    Product
    FORD — FORD F-650 SD, F-750 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·149-2015·2015-12-22

    Bellisio Recalls Boston Market Pork Rib Entrees Due To Foreign Matter

    Bellisio Foods is recalling Boston Market boneless pork rib frozen entrees due to possible glass or hard plastic contamination. No injuries have been reported.

    Product
    Bellisio Foods, Inc. — Bellisio Foods, Inc. Recalls Boneless Pork Rib Frozen Entree Products Due To Possible Foreign Matter Adulteration
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·15V856000·2015-12-21

    Starcraft RV Recalls 2015-2016 Trailers for Missing Sewer Valve Label

    Starcraft RV is recalling 2015-2016 Autumn Ridge and Solstice fifth wheel trailers because a missing caution label may allow sewer gas to enter the vehicle.

    Product
    STARCRAFT RV FW — STARCRAFT RV FW, STARCRAFT RV TT SOLSTICE, AUTUMN RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide