The Recall Desk

State

Minnesota product recalls

72,913 recalls have nationwide distribution and so reach Minnesota. 7,804 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total
7,804
Critical
1,125
Severe
1,892
Most recent
2026-09-09

Of the 7,804 recalls naming Minnesota we have scored against our rubric, 1,125 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,892 (24%) are Severe.

Which agencies issued them

These figures cover only the 7,804 recalls whose distribution notice names Minnesota specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1651–1675 of 80717

  • ModerateFDA (Drugs)·D-0599-2026·2026-06-10

    Xyvona 3 mg levorphanol tablets recalled after proprietary name denial

    Xyvona levorphanol tartrate tablets, 3 mg, are being recalled following FDA's denial of marketing the product under the proprietary name Xyvona.

    Product
    Xyvona (levorphanol tartrate tablets), 3mg, 100 Tablets, Rx only, Forte BioPharma, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Distributed by: Fort Bio-Pharma, LLC., Las Vegas, NV 89113, NDC 72245-058-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0598-2026·2026-06-10

    Xyvona levorphanol tablets recalled after FDA denied the proprietary name

    Xyvona levorphanol tartrate tablets, 2 mg, are being recalled following FDA's denial of marketing the product under the proprietary name Xyvona.

    Product
    Xyvona (levorphanol tartrate tablets), 2mg, 100 Tablets, Rx only, Forte BioPharma, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Distributed by: Fort Bio-Pharma, LLC., Las Vegas, NV 89113, NDC 72245-762-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2266-2026·2026-06-10

    B. Braun Harris Methodist kits contain Mastisol with cracking tubing

    B. Braun CESK Harris Methodist kits are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering the product unusable.

    Product
    Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK HARRIS METHODIST Model/Catalog Number: 555498 Software Version: N/A Product Description: CESK HARRIS METHODIST Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-1009-2026·2026-06-10

    Albertsons Old Bay seasoned shrimp omits shrimp declaration

    Albertsons store-made Shrimp P&D Old Bay Seasoned is being recalled because the contains statement does not declare shrimp. Five units are affected.

    Product
    UPC 23036500000 SHRIMP P&D OLD BAY SEASONED This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2305-2026·2026-06-10

    Vascular Access Dressing Recalled Due to Lack of Sterility Assurance

    DeRoyal Industries Inc. is recalling Covaderm Plus Vascular Access Dressings because they lack sterility assurance.

    Product
    DeRoyal Industries Inc. Ref 46-406, Covaderm Plus, Vascular Access Dressing 6"x6" (15cmx15cm)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-1010-2026·2026-06-10

    Albertsons cilantro lime shrimp skewers omit shrimp declaration

    Albertsons store-made Cilantro Lime Shrimp Skewers are being recalled because the contains statement does not declare shrimp.

    Product
    UPC 23070400000 SHRIMP SKEWER MEDIUM RAW CILANTRO LIME This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-1067-2026·2026-06-10

    Albertsons citrus lemon salmon fillet omits salmon declaration

    Albertsons store-made Salmon Fillet with Citrus Lemon Marinade is being recalled because the contains statement does not declare salmon.

    Product
    UPC 23151700000 SALMON FILLET With CITRUS LEMON MARINADE This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0966-2026·2026-06-10

    Albertsons Boston almond cake omits almond from contains statement

    Albertsons store-made Cake Boston Almond is being recalled because the contains statement does not declare almond. Nine units are affected.

    Product
    UPC 22749800000 CAKE BOSTON ALMOND This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2272-2026·2026-06-10

    Covidien Mon-a-Therm general purpose temperature probes lack FDA clearance

    Covidien Mon-a-Therm General Purpose Temperature Probes, REF 90044, are being recalled because the devices lack FDA clearance. 1,775 units are affected.

    Product
    Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-1070-2026·2026-06-10

    Albertsons sweet chili kosher salmon omits salmon declaration

    Albertsons store-made Salmon Sweet Chili Kosher is being recalled because the contains statement does not declare salmon.

    Product
    UPC 21877300000 SALMON SWEET CHILI KOSHER PO SS COLD This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0997-2026·2026-06-10

    Albertsons southwest shrimp bowls omit shrimp from contains statement

    Albertsons store-made Southwest Shrimp Bowls are being recalled because the contains statement does not declare shrimp. 23 units in total are affected.

    Product
    UPC 21467900000 Ready Meals BOWL SOUTHWEST SHRIMP LARGE SS COLD UPC 21963600000 Ready Meals SOUTHWEST SHRIMP BOWL SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2285-2026·2026-06-10

    Philips Azurion 3M15 Medical Imaging Systems Recalled Due to Software Issue

    Philips Medical Systems is recalling 27 Philips Azurion 3M15 units because a software issue can cause unusable dark images during imaging procedures.

    Product
    Philips Azurion 3M15, Model Numbers: 722064, 722222 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0892-2026·2026-06-10

    Yunker herbal energy supplement does not meet its vitamin E claim

    Yunker Energy & Health Herbal Supplement with Vitamins is being recalled because the product does not meet its label claim for Vitamin E. 25,130 units are affected.

    Product
    Yunker(branded) Energy & Health Herbal Supplement with Vitamins; Manufactured by Sato Pharmaceuticals Co. Ltd.; 30ml container. Packed in single serving, 3 units/pack, and 10 units per pack. Single UPC: 49873-916-11 3pack UPC: 49873-916-15 10pack UPC: 49873-916-07
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-1065-2026·2026-06-10

    Albertsons carne asada marinade salmon fillet omits salmon declaration

    Albertsons store-made Salmon Fillet Carne Asada Marinade is being recalled because the contains statement does not declare salmon. Six units are affected.

    Product
    UPC 23077600000 SALMON FILLET CARNE ASADA MARINADE This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-1001-2026·2026-06-10

    Albertsons pollo asada marinated shrimp kabobs omit shrimp declaration

    Albertsons store-made Shrimp 16-20 Kabob Pollo Asada Marinade is being recalled because the contains statement does not declare shrimp. Four units are affected.

    Product
    UPC 23043800000 SHRIMP 16-20 KABOB POLLO ASADA MARINADE This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2273-2026·2026-06-10

    Covidien 9 Fr Mon-a-Therm temperature probes lack FDA clearance

    Covidien Mon-a-Therm general purpose temperature probes in size 9 Fr, REF 90050, are being recalled because the devices lack FDA clearance. 128,900 units are affected.

    Product
    Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V371000·2026-06-09

    Ford Recalls 2024 Explorers for Potential Park System Damage

    Ford is recalling 2024 Explorer vehicles with 2.3L engines and 10R60 transmissions because an unintentional powertrain control module reset may damage the park system, increasing the risk of vehicle rollaway.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V376000·2026-06-09

    Ford Recalls Focus and Fusion Vehicles for Transmission Clutch Fracture Risk

    Ford is recalling 2015-2018 Focus and 2013-2016 Fusion vehicles previously repaired incorrectly under prior recalls. The clutch may fracture, causing transmission damage and fluid leaks that increase fire risk.

    Product
    FORD — FORD FOCUS, FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V378000·2026-06-09

    Ford Recalls 2014 F-150s for Transmission Software Update

    Ford is recalling 2014 F-150 vehicles previously repaired under recall 24V444 because a signal loss can cause unexpected downshifting, increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E033000·2026-06-09

    Cummins CNG Fuel System Recall for Tank Bracket Deformation Risk

    Natural Gas Fuel Systems is recalling Cummins CNG fuel systems because the tank support bracket may deform in a side impact, potentially causing the tank to detach and leak fuel.

    Product
    FUEL SYSTEM, OTHER:STORAGE:TANK ASSEMBLY:MOUNTING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V369000·2026-06-09

    Ford Recalls 2012-2018 Focus Vehicles for Engine Stall Risk

    Ford is recalling 2012-2018 Focus vehicles previously repaired under recall 18V735 because a malfunctioning Canister Purge Valve may cause the engine to stall while driving, increasing crash risk.

    Product
    FORD — FORD FOCUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V380000·2026-06-09

    Midwest Automotive Design motorhome ground cables may be undersized

    Alliance RV is recalling certain Midwest Automotive Design recreational vehicles because the ground wire may be undersized for the electrical system, risking overheating and fire.

    Product
    MIDWEST AUTOMOTIVE DESIGN — MIDWEST AUTOMOTIVE DESIGN ULTIMATE TRAVELER, PROFESSIONAL SERIES, ATHLETIC SERIES, BUSINESS CLASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V377000·2026-06-09

    Ford Recalls 2019 Lincoln Nautilus for Lane Center Assist Software Defect

    Ford is recalling 2019 Lincoln Nautilus vehicles previously repaired under recall 19V031 because the lane center assist system may fail to detect if the driver's hands are off the steering wheel for a prolonged period.

    Product
    LINCOLN — LINCOLN NAUTILUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V375000·2026-06-09

    Ford Recalls 2018 F-150s for Transmission Software Defect

    Ford is recalling 2018 F-150 vehicles previously repaired under recall 17V669 due to a software defect that may cause unintended gear selection and loss of gear indication.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide