The Recall Desk

State

Minnesota product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35051–35075 of 81587

  • ModerateFDA (Drugs)·D-0143-2020·2019-10-23

    Aurobindo Recalls Amphetamine Mixed Salts Tablets for Out-of-Specification Weight

    Aurobindo Pharma USA Inc. is recalling 11,129 bottles of 20mg Amphetamine Mixed Salts tablets because they failed weight and thickness specifications.

    Product
    DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0146-2020·2019-10-23

    Ingenus Recalls Leucovorin Calcium Injection Due to Crystallization

    Ingenus Pharmaceuticals is recalling Leucovorin Calcium Injection vials due to the presence of particulate matter identified as API crystallization.

    Product
    Leucovorin Calcium Injection, USP 500 mg*/50 mL (10 mg/mL) 50 mL Single-Dose Vial NDC 50742-464-50 Rx Only Ingenus Pharmaceuticals, LLC. Orlando, FL 32839
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0154-2020·2019-10-23

    Vital Scientific Viva-JR Automated Chemistry Analyzer Recalled for Power Supply Failure

    Vital Scientific N.V. is recalling four Viva-JR automated chemistry analyzers due to power supply failures that cause instrument malfunction and prevent the production of patient results.

    Product
    Viva - JR, catalog # 6002-940, UDI # 03661540600210 Product Usage: automated chemistry analyzer intended for clinical use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0035-2020·2019-10-23

    Arcadia Trading Recalls Dried Mushroom Bags for Undeclared Sulfites

    Arcadia Trading Inc. is recalling 1,425 bags of dried mushrooms because they contain undeclared sulfites. The product was distributed to a New York distributor and further distributed in seven states.

    Product
    Dried Mushroom NET WT: 8oz (227g) Ingredients: Mushroom Distributed By: Arcadia Trading Inc. Brooklyn, NY 11211. USA Product of China UPC: 791804603091
    Category
    Food
    Distribution
    7 states
  • LowFDA (Devices)·Z-0152-2020·2019-10-23

    Roche Diagnostics Recalls cobas Integra Albumin Gen.2 Test Kits

    Roche Diagnostics is recalling cobas Integra Albumin Gen.2 test kits due to low quality control recovery and invalid calibration.

    Product
    Roche Diagnostics cobas Integra Albumin Gen.2 Catalog Number: 05166861190 - Product Usage: In vitro test for the quantitative determination of the albumin in human serum and plasma on Roche/Hitachi cobas c systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0142-2020·2019-10-23

    KVK-Tech Recalls Methylphenidate Hydrochloride Oral Solution Due to Foreign Particles

    KVK-Tech is recalling 384 bottles of Methylphenidate Hydrochloride Oral Solution because of the presence of fiber particles.

    Product
    Methylphenidate Hydrochloride Oral Solution 5mg per 5mL, 500 mL Bottle, Sugar Free Alcohol Free, Rx Only, Mfd by: KVK Tech, Inc., Newtown, PA 18940, NDC 10702-0163-50.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0153-2020·2019-10-23

    Roche Cobas c Bilirubin Total Gen.3 Recalled for Quality Control Issues

    Roche Diagnostics is recalling 2,304 units of the Cobas c Bilirubin Total Gen.3 in vitro test due to low quality control recovery and invalid calibration.

    Product
    Cobas c Bilirubin Total Gen.3 Catalog Number: 05795419190 - Product Usage: In vitro test for the quantitative determination of the total bilirubin in serum and plasma of adults and neonates on Roche/Hitachi cobas c systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20010·2019-10-22

    Blackhawk T-Series L2C Gun Holsters Recalled for Injury Hazard

    Federal Cartridge is recalling Blackhawk T-Series L2C gun holsters because the design can accidentally change a firearm's safety switch, posing an injury risk.

    Product
    Blackhawk T-Series L2C gun holsters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V753000·2019-10-21

    Airstream Recalls Trailers Due to Coupler Welding Defect

    Airstream is recalling 2019-2020 travel trailers because improper welding may cause the coupler to separate from the tow ball, increasing crash risk.

    Product
    AIRSTREAM — AIRSTREAM GLOBETROTTER, FLYING CLOUD, INTERNATIONAL, SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E073000·2019-10-21

    H&H Sports Recalls VCAN V531 Motorcycle Helmets for Retention Failure

    H&H Sports Protection is recalling VCAN V531 motorcycle helmets sold on Amazon because the retention system may fail, allowing the helmet to separate from the head during a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·102-2019·2019-10-18

    George's Prepared Foods Recalls Ready-to-Eat Pork and Turkey Sausage Patties

    George's Prepared Foods is recalling approximately 6,444 pounds of ready-to-eat pork and turkey sausage patties due to possible Salmonella contamination.

    Product
    Gold Creek Foods, LLC — George's Prepared Foods Recalls Ready-To-Eat Pork and Turkey Products due to Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·20704·2019-10-18

    Soft Play Recalls Spider Climb Playground Climbers Due to Fall Hazard

    Soft Play LLC is recalling Spider Climb playground climbers installed in McDonald's restaurants due to a fall hazard. The platforms are spaced too far apart, posing a risk to children.

    Product
    Spider Climb playground climbers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V749000·2019-10-18

    Collins Recalls 2018-2019 School Buses Lacking Rear Backup Cameras

    Collins Bus Corporation is recalling 2018-2019 TL400, TL408, TH400, and TH408 school buses that may lack rear backup cameras, increasing crash risk.

    Product
    COLLINS — COLLINS TL408, TH400, TH408, TL400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V743000·2019-10-18

    Subaru Recalls Impreza and Crosstrek for Electrical Software Defect

    Subaru is recalling 2017-2019 Impreza and 2018-2019 Crosstrek vehicles because a software defect may cause the engine to stall while driving, increasing crash risk.

    Product
    SUBARU — SUBARU IMPREZA, CROSSTREK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V751000·2019-10-18

    Vac-Tron Recalls 2015-2019 LP 873 SD Trailers Due to Sway Risk

    Vac-Tron is recalling 2015-2019 LP 873 SD heavy trailers because they may sway while being towed, increasing the risk of a crash.

    Product
    VAC-TRON — VAC-TRON LP 873 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V750000·2019-10-18

    Polaris Recalls 2015-2019 Slingshot Motorcycles for Electrical Fuse Defect

    Polaris is recalling 2015-2019 Slingshot motorcycles because excessive electrical current may damage battery fuse terminals, potentially causing loss of lighting or power steering and increasing crash risk.

    Product
    POLARIS — POLARIS SLINGSHOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V741000·2019-10-17

    Toyota Recalls Vehicles Due to Airbag Inflator Explosion Risk

    Toyota is recalling approximately 928,220 vehicles because previously replaced airbag inflators may explode due to propellant degradation, posing a risk of serious injury or death.

    Product
    LEXUS — LEXUS, TOYOTA, SCION IS 350C, SC430, IS 250, IS 350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V740000·2019-10-17

    Yetti Trailers Recalled for Missing Spindle Nut Retainer Clips

    Voyager Industries is recalling 2018-2020 Yetti trailers because missing retainer clips may allow spindle nuts to loosen, potentially causing the wheel to come off the axle.

    Product
    YETTI — YETTI TRAXX, GRAND ESCAPE, ANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide