The Recall Desk

State

Minnesota product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50526–50550 of 81675

  • HighFDA (Devices)·Z-0721-2017·2016-12-14

    RayStation Radiation Therapy Software Recalled for Dose Calculation Errors

    RaySearch Laboratories is recalling RayStation software versions 4.0, 4.5, 4.7, and 5.0 due to potential inaccuracies in proton dose calculations for specific treatment plans.

    Product
    RayStation 4.0, 4.5, 4.7 and 5.0; Radiation Therapy Treatment Planning System Product Usage: RayStation is a software system designed for treatment planning and analysis of radiation therapy. The treatment plans provide treatment unit set-up parameters and estimates of dose…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0680-2017·2016-12-14

    Olympus Vanta Analytical X-Ray System Recalled for Unintentional Emission Risk

    Olympus is recalling 41 Vanta Analytical X-Ray Systems due to a risk of unintentional x-ray emission if users attempt to terminate the sequence early.

    Product
    Olympus Scientific Solutions Americas Corporation (OSSA) Model: VANTA Analytical X-Ray System
    Category
    Medical Device
    Distribution
    16 states
  • HighNHTSA·16V896000·2016-12-14

    DRV Recalls 2017 Full House Trailers Due to Door Hinge Weld Defect

    DRV Suites is recalling 2017 Full House recreational trailers because rear cargo door hinge welds may be insufficient, causing the door to swing down with excessive force.

    Product
    DRV — DRV FULL HOUSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0623-2017·2016-12-14

    Green Dirt Farm Sheep's Milk Cheese Recalled for Staphylococcus Aureus Contamination

    Green Dirt Farm is recalling "Dirt Lover" sheep's milk cheese due to Staphylococcus aureus contamination exceeding action limits.

    Product
    Green Dirt Farm "Dirt Lover" sheep's milk cheese packaged in cases of 8, 4-6 oz.. units, sold by case weight. Made by Green Dirt Farm, LLC, Weston, MO 64098.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0706-2017·2016-12-14

    Philips Spectral CT Software Recalled for Image Processing Defects

    Philips Medical Systems is recalling Spectral CT software due to a defect causing issues with filming, saving, and annotating images.

    Product
    Philips Spectral CT Applications supports viewing and analysis of images at energies selected from the available spectrum in order to provide information about the chemical composition of the body materials and/or contrast agents.
    Category
    Medical Device
    Distribution
    7 states
  • HighFDA (Food)·F-0622-2017·2016-12-14

    Green Dirt Farm Ruby Blended Milk Cheese Recalled for Staphylococcus Aureus

    Green Dirt Farm is recalling Ruby blended milk cheese due to Staphylococcus aureus contamination exceeding action limits.

    Product
    Green Dirt Farm "Ruby" blended milk cheese packaged in cases of 6, 10 - 12 oz.. units, sold by case weight. Made by Green Dirt Farm, LLC, Weston, MO 64098.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0720-2017·2016-12-14

    RayStation 5.0 Radiation Therapy Software Recalled for Dose Display Error

    RaySearch Laboratories is recalling RayStation 5.0 software due to a potential error in dose display on auxiliary CT images, which could result in incorrect treatment planning data.

    Product
    Radiation Therapy Treatment Planning System Product Usage: RayStation is a software system designed for treatment planning and analysis of radiation therapy. The treatment plans provide treatment unit set-up parameters and estimates of dose distributions expected during the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0562-2017·2016-12-14

    SSI-GoPicnic Turkey and Cheese Snacks Recalled for Gluten Mislabeling

    SSI-GoPicnic LLC is recalling 1,584 cartons of Turkey Slices & Cheddar Cheese snacks labeled gluten-free because they contain wheat gluten.

    Product
    GoPicnic Turkey Slices & Cheddar Cheese; 4 Individually Packed Snacks; GLUTEN FREE; Best by: 31 JAN 2017
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0657-2017·2016-12-14

    Saputo Recalls Low Moisture Mozzarella Cheese Due to Foreign Material

    Saputo Cheese USA is recalling specific lots of low moisture mozzarella cheese after a customer reported finding white plastic in the product.

    Product
    MOZZARELLA LOW MOISTURE WHOLE MILK 8/6# DRAGONE ; Low moisture Mozzarella Cheese Pasteurized Milk, Cheese Cultures, Salt, Enzymes. UPC: #070348121002 Saputo code: #112100
    Category
    Food
    Distribution
    24 states
  • ModerateFDA (Food)·F-0676-2017·2016-12-14

    Airheads Mini Bars Recalled Due to Blood Observed on Packaging Equipment

    Perfetti Van Melle USA Inc is recalling Airheads Mini Bars because blood was observed on packaging equipment. The recall covers 4,147 cases distributed nationwide.

    Product
    Airheads Mini Bars 12oz bags of assorted flavors. 12 - 12oz bags are included in cardboard cartons. Assorted flavors include Cherry, Watermelon, Blue Raspberry, and White Mystery.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0708-2017·2016-12-14

    Navilyst Recalls Xcela PICC Kits Due to Incorrect Glove Expiration Dates

    Navilyst Medical is recalling Xcela Power Injectable PICC Maximal Barrier Nursing Kits because included sterile gloves have incorrect expiration dates.

    Product
    Xcela Power Injectable PICC Maximal Barrier Nursing Kit The Maximal Barrier Nursing Kits are Tandem Pack Convenience Kits packaged with a NMI PICC and accessories. The Xcela Power Injectable PICC is indicated for short or long-term peripheral access to the central venous system…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0724-2017·2016-12-14

    Halyard C-Section Drapes Recalled for Manufacturing Variation

    Halyard Health is recalling specific lots of C-Section drapes because a manufacturing variation may prevent the removal of coated release paper, inhibiting easy access to the surgical site.

    Product
    Halyard C-Section Drape with Clear Screen and Full Incise (Non-Sterile), Product Code 44965 NS; C-Section Drape with Clear Screen and Full Incise (Sterile), Product Code 44966 00; C-Section Drape with Clear Screen (Non-Sterile), Product Code 44967 NS; C-Section Drape with Clear…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0714-2017·2016-12-14

    Angiodynamics Recalls PICC Catheters Due to Stylet Diameter Labeling Error

    Angiodynamics Inc. is recalling specific PICC catheters because the stylet diameter may differ from the label, potentially causing stiffening.

    Product
    Peripherally Inserted Central Catheters (PICC), UPN H965750141, Catalog # 75-014 The Maximal Barrier Nursing Kits are Tandem Pack Convenience Kits packaged with a NMI PICC and accessories. The BioFlo PICC with ENDEXO Technology and BioFlo PICC with ENDEXO and PASV Valve…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0716-2017·2016-12-14

    Sorin Perceval Sutureless Aortic Heart Valve Field Action

    Sorin Group USA is conducting a voluntary field action for Perceval Sutureless Aortic Heart Valves due to updated implantation procedure steps.

    Product
    Perceval Sutureless Aortic Heart Valve size S, Item # ICV1208, REF PVS21; Perceval Sutureless Aortic Heart Valve size M, Item # ICV1209, REF PVS23; Perceval Sutureless Aortic Heart Valve size L, Item # ICV1210, REF PVS25; Perceval Sutureless Aortic Heart Valve size XL, Item #…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0666-2017·2016-12-14

    Saputo Recalls Whole Milk Cheese Due to Foreign Material

    Saputo Cheese USA is recalling specific lots of Vesuvio Bella Whole Milk Cheese after a customer reported finding white plastic in the product.

    Product
    WHOLE MILK CHEESE 8/6# VESUVIO BELLA; Pasteurized Milk, Cheese Cultures, Salt, Enzymes. Distributed by US Foods UPC: #075805891658 Saputo code: #989165
    Category
    Food
    Distribution
    24 states
  • ModerateFDA (Devices)·Z-0712-2017·2016-12-14

    DeRoyal Recalls PneuGel Tennis Elbow Supports Due to Mold Complaints

    DeRoyal Industries is recalling 56 units of PneuGel tennis elbow supports because of complaints regarding mold on the straps.

    Product
    TENNIS ELBOW SUPPORT, PneuGel(TM), UNIVERSAL, REF 200A10, QTY: 1 Each, Rx Only, Product Usage: Lateral and medial epicondylitis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0709-2017·2016-12-14

    BioFlo PICC Nursing Kits Recalled for Incorrect Glove Expiration Dates

    Navilyst is recalling BioFlo PICC Maximal Barrier Nursing Kits because the included sterile gloves have incorrect expiration dates.

    Product
    BioFlo PICC with ENDEXO Technology Maximal Barrier Nursing Kit - 1) UPN # H965750121/Catalog No: 5018265, 2) UPN # H965750131/Catalog No:5024787, 3) UPN # H965750141/Catalog No: 5024787, 4) UPN # H965750241/Catalog No: 5020644, 5) UPN # H965750325/Catalog No: 5026458, 6) UPN #…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0663-2017·2016-12-14

    Saputo Whole Milk Mozzarella Cheese Recalled for Foreign Material

    Saputo is recalling specific lots of Whole Milk Mozzarella cheese after a customer reported finding white plastic in the product.

    Product
    WHOLE MILK CHEESE 8/6# MOZZERIA - Saputo; Pasteurized Milk, Cheese Cultures, Salt, Enzymes. UPC: #075805888948 Saputo code: #988947
    Category
    Food
    Distribution
    24 states
  • ModerateFDA (Food)·F-0662-2017·2016-12-14

    Saputo Recalls Mozzarella Cheese Due to Foreign Material Complaint

    Saputo Cheese USA is recalling specific lots of low-moisture mozzarella cheese after a customer reported finding white plastic in the product.

    Product
    MOZZARELLA LOW MOISTURE WHOLE MILK 8/6# CHEESECAKE FACTORY TCCFI; Pasteurized Milk, Cheese Cultures, Salt, Enzymes. UPC: # #075805884759 Saputo code: #988475
    Category
    Food
    Distribution
    24 states
  • ModerateFDA (Food)·F-0615-2017·2016-12-14

    Cre 8 It Stuffing Recalled Due to Temperature Control Issues

    Cre 8 It, Inc. is recalling stuffing mix after a complaint of sour taste indicated a storage thermometer error.

    Product
    Cre 8 It, Inc. Stuffing, 011951311916 in covered aluminum foil pans. Net Weight 2/4 lb. (3.63kg) containers per shipping case
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0705-2017·2016-12-14

    Philips IQon Spectral CT Software Defect Recall

    Philips is recalling 24 IQon Spectral CT systems due to a software defect that causes issues with filming, saving, and annotating images.

    Product
    IQon Spectral CT is a Computed Tomography X-Ray System intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·F-0664-2017·2016-12-14

    Saputo Recalls Mozzarella Cheese Due to Foreign Material Complaint

    Saputo Cheese USA is recalling specific lots of Mozzarella Style Low Moisture Whole Milk cheese after a complaint of white plastic found in the product.

    Product
    MOZZARELLA STYLE LOW MOISTURE WHOLE MILK 8/6# HARVEST VALUE; Pasteurized Milk, Cheese Cultures, Salt, Enzymes. UPC: #758108633766 Saputo code: #988995
    Category
    Food
    Distribution
    24 states
  • ModerateFDA (Food)·F-0660-2017·2016-12-14

    Saputo Recalls Mozzarella Cheese Due to Foreign Material Complaint

    Saputo Cheese USA is recalling specific lots of low-moisture mozzarella cheese after a customer reported finding white plastic in the product.

    Product
    MOZZARELLA LOW MOISTURE WHOLE MILK 8/6# ROSELI; Pasteurized Milk, Cheese Cultures, Salt, Enzymes. US Foods UPC: # #758108015111 Saputo code: #984639
    Category
    Food
    Distribution
    24 states
  • ModerateFDA (Food)·F-0659-2017·2016-12-14

    Saputo Mozzarella Recalled for White Plastic Contamination

    Saputo Cheese USA is recalling low-moisture mozzarella cheese after a customer reported finding white plastic in the product.

    Product
    MOZZARELLA LOW MOISTURE WHOLE MILK 8/6# CHUCK E CHEESE Pasteurized Milk, Cheese Cultures, Salt, Enzymes. UPC: # #075805845347 Saputo code: #984534
    Category
    Food
    Distribution
    24 states