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.

50426–50450 of 81675

  • HighFDA (Devices)·Z-0765-2017·2016-12-21

    Stryker Recalls Reprocessed Xcel Bladeless Trocars Due to Plug Breakage

    Stryker is recalling 40,476 reprocessed Xcel Bladeless Trocars because the adjustable plug may break in packaging or during use.

    Product
    Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed Endoscopic Trocars are indicated for use to establish a port of entry for endoscopic instruments in patients requiring minimally invasive surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V918000·2016-12-21

    Volvo Recalls 2017 S60, V60, and XC60 for Side Air Bag Defect

    Volvo is recalling 2017 S60, V60, and XC60 vehicles because side air bag inflator initiators may fail to ignite during a crash, preventing deployment.

    Product
    VOLVO — VOLVO V60, XC60, S60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V920000·2016-12-21

    Toyota Recalls 2017 86 Vehicles for Ignition Key Removal Defect

    Toyota is recalling 2017 86 vehicles with automatic transmissions and ignition keys because the key may be removed without the transmission in Park, increasing the risk of the vehicle rolling away.

    Product
    TOYOTA — TOYOTA 86
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0682-2017·2016-12-21

    Good Sense Trail Mix Recalled for Undeclared Allergens

    Waymouth Farms is recalling Good Sense Trail Mix, Cranberries 'N More, because it may contain undeclared pecans, walnuts, wheat, milk, and soy.

    Product
    Good Sense Trail Mix, Cranberries 'N More, Net Wt. 6 oz. (170g). Cranberries, Sunflower Nuts, Cashews, Pumpkin Seeds, Almonds, Apples. UPC 30243-86343.
    Category
    Food
    Distribution
    16 states
  • HighFDA (Devices)·Z-0759-2017·2016-12-21

    Telefac Medical Recalls Weck Facial Closure Systems Due to Detachment Risk

    Teleflex Medical is recalling 2,265 units of Weck Facial Closure Systems because the device wings may partially detach from the shield during use.

    Product
    Weck Facial Closure Systems have application in laparoscopic procedures for approximation of tissues and percutaneous suturing for closing incision sites.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0764-2017·2016-12-21

    Teleflex Visistat Skin Staplers Recalled for Sterility Deficiency

    Teleflex Medical is recalling Visistat 35W disposable skin staplers because improper packaging seals mean sterility is not assured.

    Product
    WECK Visistat 35W, Disposable Skin Stapler, Rx Only, Sterile, Teleflex Medical, NC 27709. The intended use of the Visistat stapler is to close lacerations on the outer layer of the dermis for a wide range of general, thoracic, obstetric, gynecological, orthopedic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0728-2017·2016-12-21

    Prism Medical Carry Bar Recall Due to Breaking Plastic Component

    Prism Medical is recalling carry bars for patient lifts because a black plastic puck may break, posing a risk of harm to patients.

    Product
    Carry bar which is an accessory to a lift used for patients in hospitals and other facilities. Recall impacts the following model numbers: 360741, 360750, 360751, 360755, 360755 Rev B, 360756, and 360757.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0766-2017·2016-12-21

    Encore Medical Recalls Empowr PS Knee System Box Cut Guides

    Encore Medical is recalling 162 Empowr PS Knee System Box Cut Guides because femoral chipping occurred during surgery.

    Product
    Empowr PS Knee System Box Cut Guide The EMPOWER PS Box Cut Guide is used to make the housing resection for the post of the posterior stabilized implant
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0731-2017·2016-12-21

    Elekta Recalls MOSAIQ Oncology Information System Due to Data Saving Error

    Elekta is recalling 47 MOSAIQ Oncology Information System units because edits to particle field definition parameters may not be saved.

    Product
    MOSAIQ Oncology Information System The product is used to manage workflows for treatment planning and delivery. It supports information flow among healthcare facility personnel and can be use wherever radiotherapy and chemotherapy are prescribed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0733-2017·2016-12-21

    Cook Medical Recalls Central Venous Catheter Trays Due to Incorrect Needles

    Cook Medical is recalling 99 units of Spectrum Minocycline/Rifampin Impregnated Central Venous Catheter Trays because they may contain incorrect needles, potentially preventing wire guide passage.

    Product
    Cook Spectrum Minocycline/Rifampin Impregnated Double Lumen Central Venous Catheter Tray Cook Spectrum Minocycline/Rifampin Impregnated Triple Lumen Central Venous Catheter Tray
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-0729-2017·2016-12-21

    Merge Cardio software recalled for potential report matching errors

    Merge Healthcare is recalling Merge Cardio software versions 8.30.0 through 10.1.1 because images sent without an order may be matched to the wrong accession number.

    Product
    Merge Cardio software. Merge Cardio is a system intended to be used to acquire, store, print, transfer, and archive clinical information including images, Hemodynamic studies and reports, measurements (via import from DICOM Structured Reporting, text files or optical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0743-2017·2016-12-21

    Cargill Recalls Crisco Professional Liquid Butter Alternative for Excessive Additives

    Cargill is recalling Crisco Professional Liquid Butter Alternative because it contains excessive amounts of TBHQ and DMPS. The product was distributed to 29 states.

    Product
    Crisco PROFESSIONAL Liquid Butter Alternative, SALTED FOR ADDED FLAVOR, NET/NETO 1 GAL (3.79 L) INGREDIENTS; Corn Oil, Soybean Oil, Sunflower Oil, Hydrogenated Soybean Oil, Salt, Soy Lecithin***TBHQ ***Dimethylpolysiloxane***CONTAINS: SOY. UPC 7 81525 64775 7
    Category
    Food
    Distribution
    29 states
  • HighFDA (Devices)·Z-0755-2017·2016-12-21

    GE Healthcare Recalls Avance and Amingo Anesthesia Devices Due to Malfunction Risk

    GE Healthcare is recalling specific Avance CS2, Avance, and Amingo anesthesia devices because they may enter a System Malfunction state if a storage drawer closes with excessive force.

    Product
    GE Healthcare, Avance, Avance CS2, Amingo.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0732-2017·2016-12-21

    GF Health Products Recalls Patriot Homecare Beds Due to Motor Defect

    GF Health Products is voluntarily correcting Patriot homecare beds because contaminated motor housings may crack, potentially causing the head section to fall.

    Product
    Lumex, Patriot Full Electric Homecare Bed, & Patriot LX Full Electric Homecare Bed containing the Okin Dumat 3 Head/Foot Motors. Description Part Number Motor and Pendant Patriot Full Electric 120V…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0734-2017·2016-12-21

    Accuray Recalls CyberKnife Systems Due to Unexpected Robot Motion

    Accuray is recalling 40 CyberKnife Robotic Radiosurgery Systems with software version 10.6 due to a potential safety issue involving unexpected treatment robot motion when removing an accessory.

    Product
    CyberKnife Robotic Radiosurgery System using software version 10.6; Catalog/Part Number: 54000 UDI: M658053301 0 Radiology: The CyberKnife Robotic Radiosurgery System is indicated for treatment planning and image guided stereotactic Radiosurgery and precision radiotherapy…
    Category
    Medical Device
    Distribution
    12 states
  • ModerateFDA (Devices)·Z-0770-2017·2016-12-21

    Natus neoBLUE blanket LED Phototherapy System Recalled for Fiber Optic Degradation

    Natus Medical is recalling neoBLUE blanket LED Phototherapy Systems due to discoloration and degradation of the fiberoptic bundle at the pad and box connection.

    Product
    Natus neoBLUE blanket LED Phototherapy system, neonatal phototherapy. Used to provide treatment for neonatal Hyperbilirubinemia. 006224 neoBLUE blanket LED Phototherapy Systems with Large blanket/pad 006254 neoBLUE blanket LED Light Box 006895 neoBLUE blanket LED…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0748-2017·2016-12-21

    Ellman Minor Surgery Bipolar Cable Recalled for Mismatched Expiration Dates

    Ellman International is recalling 370 boxes of Minor Surgery Bipolar Cables because the expiration dates on the outer boxes and individual pouches do not match.

    Product
    ellman A CYNOSURE COMPANY Minor Surgery Bipolar Cable, Contents: Five (5) Disposable Bipolar Cables,STERILE The Minor Surgery Bipolar Cable is an accessory that is used to connect the bipolar handpieces to the RF generator for electrosurgical procedures that require the bipolar…
    Category
    Medical Device
    Distribution
    12 states
  • ModerateFDA (Devices)·Z-0730-2017·2016-12-21

    Merge Cardio software recall for data loss during inactivity

    Merge Healthcare is recalling Merge Cardio software versions 10.1 and 10.1.1 because the reporting feature times out after one hour of inactivity, causing data loss.

    Product
    Merge Cardio software. Merge Cardio is a system intended to be used to acquire, store, print, transfer, and archive clinical information from Camtronics and other vendors systems including images, hemodynamic studies and reports, measurements (via import from DICOM…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0758-2017·2016-12-21

    Halyard Health Recalls Sterling Nitrile Sterile Exam Gloves Due to Defects

    Halyard Health is recalling Sterling Nitrile Sterile Powder Free Exam Gloves because they may be discolored and brittle, causing them to tear when put on.

    Product
    Sterling Nitrile Sterile Powder Free Exam Gloves, S, Sterile.
    Category
    Medical Device
    Distribution
    13 states
  • ModerateFDA (Food)·F-0744-2017·2016-12-21

    Cargill Recalls Butter Flavored Oil Due to Excessive Additives

    Cargill is recalling 1-gallon bottles of refyne Butter Flavored Oil because they contain excessive amounts of TBHQ and dimethyl polysiloxane.

    Product
    refyne Artificially Flavored BUTTER FLAVORED OIL, NET CONTENTS 1 GAL (3.79 L) INGREDIENTS; SOYBEAN OIL, HYDROGENATED SOYBEAN OIL,***TBHQ--- Dimethylpolysiloxane***CONTAINS: SOY., UPC 0 41560 13659 4
    Category
    Food
    Distribution
    29 states
  • ModerateFDA (Devices)·Z-0743-2017·2016-12-21

    Siemens SOMATOM Definition Flash CT Systems Recalled for Software Update

    Siemens is recalling 104 SOMATOM Definition Flash CT systems to install a software and firmware update that fixes bugs and improves performance.

    Product
    SOMATOM Definition Flash System, x-ray, tomography, computed Intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes taken at different angles
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0735-2017·2016-12-21

    C.R. Bard Recalls 70cc Irrigation Syringes Due to Package Defect

    C.R. Bard is recalling 452,728 units of 70cc irrigation syringes because a package defect may compromise product sterility.

    Product
    BARD¿ Irrigation, Syringe 70cc With Resectoscope Tip, Catheter Tip, Luer Adapter And Cap, Rx Only, Sterile, The BARD¿ Syringe is available in a single use plastic design which features a 60cc or 70cc capacity graduated barrel. It has a thumb ring plunger for one-handed use. A…
    Category
    Medical Device
    Distribution
    Distributed nationwide