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.

55251–55275 of 81678

  • SevereFDA (Food)·F-0767-2016·2016-03-23

    Wilderness Family Naturals Coconut Milk Powder Recalled for Milk Contamination

    Wilderness Family Naturals is recalling Organic Coconut Milk Powder and related products due to potential milk contamination.

    Product
    Morning Star Disaster Supplies Creamy Coconut Rice Soup, Net Wt 7.25 oz (206 g). UPC 853328-006038, Foil Bag Wilderness Family Naturals Quick Meal Creamy Coconut Rice Soup, Net Wt 7.25 oz (206 g). UPC 853328-006038, Foil Bag
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0771-2016·2016-03-23

    Wilderness Family Naturals Coconut Milk Powder Recalled for Milk Contamination

    Wilderness Family Naturals is recalling Organic Coconut Milk Powder and related soup products due to potential milk contamination.

    Product
    Morning Star Disaster Supplies Creamy Mushroom Wild Rice Soup, Net Wt 7.3 oz (207 g). UPC 853328-006045, Foil Bag Wilderness Family Naturals Quick Meal Creamy Mushroom Wild Rice Soup Mix, Net Wt 7.3 oz (207 g). UPC 898392-007994, Foil Bag
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0764-2016·2016-03-23

    Wilderness Family Naturals Organic Coconut Milk Powder Recalled for Milk Contamination

    Wilderness Family Naturals is recalling Organic Coconut Milk Powder and related products due to potential milk contamination.

    Product
    Morning Star Disaster Supplies Quick Meal Mexican Corn Soup Mix Net Wt. 8.1 oz (230g)., Foil Bag. UPC 853328-006090 Wilderness Family Naturals Quick Meal Mexican Corn Soup Mix., Net Wt 8.1 oz (230 g)., Foil Bag. UPC 898392-007949
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0757-2016·2016-03-23

    Wilderness Family Naturals Coconut Milk Powder Recalled for Milk Contamination

    Wilderness Family Naturals is recalling Organic Coconut Milk Powder and products containing it due to potential milk contamination.

    Product
    Wilderness Family Naturals Coconut Milk, Powdered, Organic packaged in the following sizes: 1) 16 oz foil pouch, UPC 98392-00769; 2) 12 lb. Case of 12 - 1 lbs packages, UPC 01002457 3) 5 lb. bag, UPC 98392-00770 4) 30 lb. Case of 6 - 5 lb. packages, UPC 01002458 5) Case…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0770-2016·2016-03-23

    Wilderness Family Naturals Coconut Milk Powder Recalled for Milk Contamination

    Wilderness Family Naturals is recalling Organic Coconut Milk Powder and related products due to potential milk contamination.

    Product
    Morning Star Disaster Supplies Broccoli Potato Soup Mix, Net Wt 6.91 oz (196 g). UPC 853328-006014, Foil Bag Wilderness Family Naturals Quick Meal Broccoli Potato Soup Mix, Net Wt 6.91, (196 g). UPC 898392-007963, Foil Bag
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V169000·2016-03-23

    Porsche Recalls Cayenne Vehicles Due to Brake Pedal Pivot Pin Defect

    Porsche is recalling 2011-2016 Cayenne vehicles because a missing circlip may allow the brake pedal to dislodge, potentially preventing the driver from braking.

    Product
    PORSCHE — PORSCHE CAYENNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0758-2016·2016-03-23

    Wilderness Family Naturals Organic Hot Chocolate Mix Recalled for Milk Contamination

    Wilderness Family Naturals is recalling Organic Hot Chocolate Mix and other products containing Organic Coconut Milk Powder due to potential milk contamination.

    Product
    Wilderness Family Naturals Cacao, Organic Hot Chocolate Mix Packaged in the following sizes: 1 lb. Foil Bag, UPC 898392-007765; 12 lb. (12 - 1 lb. Foil Bags in a cardboard box), UPC 01002464; 5 lb. Foil Bag, UPC 898392-007772; and 30 lb. (6-5lb. Foil Bags in a…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0768-2016·2016-03-23

    Wilderness Family Naturals Coconut Curry Recalled for Milk Contamination

    Wilderness Family Naturals is recalling specific Coconut Vegetable Curry over Quinoa products due to potential milk contamination.

    Product
    Morning Star Disaster Supplies Coconut Vegetable Curry over Quinoa, Net Wt 4.95 oz (115 g). UPC 853328-006069, Foil Bag Wilderness Family Naturals Quick Meal Coconut Vegetable Curry over Quinoa, Net Wt 4.95 oz (115 g). UPC 853328-006229, Foil Bag
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V168000·2016-03-23

    Chrysler Recalls 2015-2016 Jeep and Dodge Vehicles for Brake Caliper Defect

    Chrysler is recalling 21,183 2015-2016 Jeep Grand Cherokee and Dodge Durango vehicles because the left front brake caliper may crack, increasing stopping distance and crash risk.

    Product
    DODGE — DODGE, JEEP DURANGO, GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0769-2016·2016-03-23

    Wilderness Family Naturals Jamaican Beans and Rice Recalled for Milk Contamination

    Wilderness Family Naturals is recalling specific lots of Jamaican Beans and Rice products due to potential milk contamination.

    Product
    Morning Star Disaster Supplies Jamaican Beans and Rice, Net Wt 8.62 oz (244 g). UPC 853328-006076, Foil Bag Wilderness Family Naturals Quick Meal Jamaican Beans and Rice, Net Wt 8.62 oz (244 g). UPC 898392-007987, Foil Bag
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0759-2016·2016-03-23

    Wilderness Family Naturals Coconut Chia Pudding Mix Recalled for Milk Contamination

    Wilderness Family Naturals is recalling Organic Coconut Chia Pudding Mix due to potential milk contamination. The product was distributed nationwide in the US and in Canada.

    Product
    Wilderness Family Naturals Coconut Chia Pudding Mix Organic, packaged in the following sizes: 1.1 lb Plastic Bag, UPC 898392-007789, and 13.2 lb. (12 plastic bags in a cardboard box) UPC 01002466
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0762-2016·2016-03-23

    Wilderness Family Naturals Coconut Milk Powder Recalled for Milk Contamination

    Wilderness Family Naturals is recalling Organic Coconut Milk Powder and related products due to potential milk contamination.

    Product
    Wilderness Family Naturals Choco Maca Strawberry Cereal Organic 8 oz.., Foil Bag UPC 898392-007819
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1185-2016·2016-03-23

    Stryker Recalls 36 Non-Powered Stretchers Due to Hydraulic Jack Assembly Defect

    Stryker is recalling 36 non-powered stretchers because hydraulic jack assemblies were manufactured with incorrect oil, increasing the risk of leaks or jack drift.

    Product
    Transport Stretcher, and Head and Neck Surgery Stretcher Non-powered stretcher
    Category
    Medical Device
    Distribution
    15 states
  • HighFDA (Devices)·Z-1148-2016·2016-03-23

    Zimmer NexGen MIS Tibia Plate Recall for Sterility Concerns

    Zimmer Manufacturing B.V. is recalling NexGen MIS Tibia Plates due to insufficient sealer calibration data, raising concerns about the sterility of the devices.

    Product
    Product 50 consists of all product under product code: JWH and same usage: Item no: 595002701 NEXGEN MIS TIBIA PLATE PR 595002702 NEXGEN MIS TIBIA PLATE PR 595003701 NEXGEN MIS TIBIA PLATE PR 595003702 NEXGEN MIS TIBIA PLATE PR 595003712 NEXGEN MIS TIBIA PLATE PR…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1161-2016·2016-03-23

    Zimmer Manufacturing Recalls Trilogy Acet Shells Due to Calibration Issues

    Zimmer Manufacturing B.V. is recalling 2,063 units of Trilogy Acet Shells used in total hip arthroplasty due to insufficient sealer calibration data.

    Product
    Product 63 consists of all product under product code: LPH and same usage: Item no: 620004020 TRILOGY ACET SHELL 40MM O 620004220 TRILOGY ACET SHELL 42MM O 620004420 TRILOGY ACET SHELL 44MM O 620004620 TRILOGY ACET SHELL 46MM O 620004621 TRILOGY ACET SHELL 46MM O…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1101-2016·2016-03-23

    Zimmer Manufacturing Recalls Unipolar Femoral Heads Due to Sterility Concerns

    Zimmer Manufacturing B.V. is recalling 2,239 unipolar femoral heads used in hip arthroplasty due to insufficient sealer calibration data, raising concerns about the sterility of the devices.

    Product
    Product 3 consists of all products under product code JDI, and same usage: Item no:781803800 12/14 UNIPOLAR FEMORAL HE 781804000 12/14 UNIPOLAR FEMORAL HE 781804100 12/14 UNIPOLAR FEMORAL HE 781804200 12/14 UNIPOLAR FEMORAL HE 781804300 12/14 UNIPOLAR FEMORAL HE 781804400…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1133-2016·2016-03-23

    Zimmer Manufacturing Recalls Sterile Knee Fluted Rods Due to Sealer Calibration

    Zimmer Manufacturing B.V. is recalling 49 units of sterile I/B II Knee Fluted Rods due to insufficient sealer calibration data.

    Product
    Product 35 consists of all product under product code: JWH and same usage: Item no: 522007300 I/B II KNEE FLUTED ROD, 1 for use in total knee arthroplasty
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V166000·2016-03-23

    Bugatti Recalls Veyron Models Due to Corroding Underbody Aluminum Plates

    Bugatti is recalling 2006-2013 Veyron models because underbody aluminum plates may corrode and detach, posing a road hazard to other vehicles.

    Product
    BUGATTI — BUGATTI VEYRON, VEYRON GRAND SPORT, VEYRON SUPER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1100-2016·2016-03-23

    Zimmer Manufacturing Recalls Hip Femoral Heads Due to Calibration Issues

    Zimmer Manufacturing B.V. is recalling 35,032 hip femoral heads due to insufficient sealer calibration data. The affected sterile products were packaged between August 2010 and April 2013.

    Product
    Product 2 consists of all products product code LPH, and same usage: 801802202 12/14 COCR FEMORAL HEAD 2 801802220 12/14 COCR FEMORAL HEAD 2 801802230 12/14 COCR FEMORAL HEAD 2 801802601 12/14 COCR FEMORAL HEAD 2 801802602 12/14 COCR FEMORAL HEAD 2 801802603 12/14 COCR…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1126-2016·2016-03-23

    Zimmer Manufacturing Recalls Sterile Femoral Hip Implant Components

    Zimmer Manufacturing B.V. is recalling specific sterile femoral hip implant components due to insufficient sealer calibration data.

    Product
    Product 28 consists of all product under product code: JDI and same usage: Item no: 32902605000 FEMORAL HD 28MM MEDIUM 32902604000 FEMORAL HD 28MM SHORT 32902604035 FEMORAL HD 28MM SHT+ 3.5M For use in total or hemi hip arthroplasty
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1172-2016·2016-03-23

    Roche Recalls Accu-Chek Inform II Base Units Due to Data Loss Risk

    Roche is recalling Accu-Chek Inform II Base Units because they may lose data or mismatch patient records when connected to specific Data Management Systems.

    Product
    Accu-Chek Inform II Base Unit as a part of the Accu-Chek Inform II Blood Glucose Monitoring System Accu-Chek inform II Blood Glucose Monitoring System is intended for testing outside the body (in vitro diagnostic use) and is intended for multiple-patient use in professional…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1137-2016·2016-03-23

    Zimmer Ion Implanted Femoral Stems Recalled for Sterility Concerns

    Zimmer Manufacturing B.V. is recalling 17 ion implanted femoral stems used in hip arthroplasty due to insufficient sealer calibration data affecting sterility.

    Product
    Product 39 consists of all product under product code: JDI and same usage: Item no: 32902605800 ION IMPLANTED FEM 22MM LO 32902604900 ION IMPLANTED FEM 26MM ME 32902603900 ION IMPLANTED FEM 26MM SH For use in total or hemi hip arthroplasty
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1176-2016·2016-03-23

    CHG Hospital Beds Recalls Spirit Select Beds Due to Alarm Defect

    CHG Hospital Beds is recalling 1,892 Spirit Select beds because the bed exit alarm may fail to function, potentially delaying assistance after a patient fall.

    Product
    The Spirit TM Select bed is a Med-Surg bed intended to support and transport low to moderate acuity patients in the medical and/or surgical area of the hospital. The Spirit Select bed is also intended for use as a general purpose, variable height hospital bed for general care…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1174-2016·2016-03-23

    Cordis Avanti Catheter Sheath Introducer System Recalled for Incorrect Cannula Size

    Cordis Corporation is recalling 1,985 units of the Avanti Catheter Sheath Introducer System because the cannula is smaller than intended.

    Product
    CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM The product includes a Catheter Sheath Introducer (CSI) and a vessel dilator. A Catheter Sheath Introducer facilitates percutaneous entry of an intravascular device. A vessel dilator facilitates the percutaneous entry of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide