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.

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.

54751–54775 of 81678

  • HighFDA (Devices)·Z-1507-2016·2016-04-27

    Stryker Recalls VariAx Compression Plating System Due to Screw Failure

    Stryker Howmedica Osteonics Corp. is recalling 118 units of the VariAx Compression Plating System because bone screws may pass through oblong holes during insertion.

    Product
    VariAx Compression Plating System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1518-2016·2016-04-27

    Siemens SOMATOM Definition CT Systems Recalled for Software Bugs

    Siemens Medical Solutions USA is recalling 1,096 SOMATOM Definition CT systems due to software bugs that may cause scan aborts, re-scans, or accidental radiation.

    Product
    Siemens SOMATOM Definition: Intended to produce cross-sectional images of the body. Computed tomography (CT) x-ray system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1511-2016·2016-04-27

    Ossur Lil Angel Vest Recalled for Potential Plastic Strap Fracture

    Ossur H / F is recalling Lil Angel Vest P2 Lambswool units because the plastic stabilizer strap may partially or completely fracture.

    Product
    Ossur Lil Angel Vest P2 Lambswool. Pediatric sized vest is a support structure used with the halo system for traumatic or chronic disorders requiring traction along the cervical spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1510-2016·2016-04-27

    Ossur Lil Angel Vest P2 Kodel Recalled for Potential Plastic Strap Fracture

    Ossur H / F is recalling 435 Lil Angel Vest P2 Kodel units due to a potential for partial or complete fracture of the plastic stabilizer strap.

    Product
    Ossur Lil Angel Vest P2 Kodel. Pediatric sized vest is a support structure used with the halo system for traumatic or chronic disorders requiring traction along the cervical spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1519-2016·2016-04-27

    Siemens SOMATOM Definition AS CT Systems Recalled for Software Bugs

    Siemens is recalling 1,096 SOMATOM Definition AS CT systems due to software bugs that may cause scan aborts, rescans, or accidental radiation.

    Product
    Siemens SOMATOM Definition AS; Intended to produce cross-sectional images of the body. Computed tomography (CT) x-ray system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1502-2016·2016-04-27

    Spacelabs Xhibit Telemetry Receiver Recall for Signal Loss

    Spacelabs Healthcare is recalling Xhibit Telemetry Receivers due to frequent signal loss that may cause offline errors on central monitors.

    Product
    The Spacelabs Healthcare Xhibit Telemetry Receiver (XTR), Model 96280 is used to transmit patient(s) physiological measurements and data to a monitor.
    Category
    Medical Device
    Distribution
    17 states
  • HighFDA (Devices)·Z-1514-2016·2016-04-27

    Ossur Lil Angel Vest Recalled for Potential Plastic Strap Fracture

    Ossur H / F is recalling Lil Angel Vest P3 Lambswool units because the plastic stabilizer strap may fracture. The recall covers 435 units distributed in the US and Hong Kong.

    Product
    Ossur Lil Angel Vest P3 Lambswool. Pediatric sized vest is a support structure used with the halo system for traumatic or chronic disorders requiring traction along the cervical spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1499-2016·2016-04-27

    Leica Surgical Microscopes Recalled for Potential Overheating and Smoke

    Leica Microsystems is recalling 381 M525 and M720 surgical microscopes because an electronic component may overheat, causing smoke and smell.

    Product
    Leica Microsystems (Schweiz) Ag. The common name of the device is surgical microscope. It has been assigned the product code FSO by the FDA and is classified as a Class I medical device. Intended for improving the visibility of objects through magnification and illumination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1525-2016·2016-04-27

    Coloplast Recalls Pediatric Catheters Due to Missing Eyelets

    Coloplast is voluntarily recalling a single lot of Self-Cath Pediatric Catheters because some units have missing eyelets, which can cause catheter malfunction.

    Product
    Self-Cath¿ Pediatric Catheter Size CH 06, Product # 5044101400, Catakig # 306. Product Usage: The Self-Cath intermittent urinary catheter discussed in this document is a pediatric size CH06 French catheter. The catheter is indicated for use by patients with chronic urine…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1113-2016·2016-04-27

    Materne Recalls GoGo squeeZ Apple Sauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.

    Product
    Gogo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12x4, Apple/Strawberry Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1115-2016·2016-04-27

    Materne Recalls GoGo squeeZ Apple Sauce Pouches Due to Residue

    Materne North America Corp is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12x4, Apple/Pear/Carrot (Zippin'Zingin'Pear) Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1106-2016·2016-04-27

    Materne Recalls GoGo squeeZ Apple Sauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12 x4, Apple/Peach Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1516-2016·2016-04-27

    Stryker GDC 360 Detachable Coils Recalled for Incorrect DFU Packaging

    Stryker Neurovascular is recalling GDC 360 Detachable Coils because an incorrect Device Form Unique (DFU) was packaged with two lots.

    Product
    GDC-10 360 SOFT 10MM X 20CM SR Detachable Coil Sterile; Model number: M0033471020SR0; Neurology: GDC 360 Detachable Coils are intended for embolization of those intracranial aneurysms that because of their morphology, their location, or the patients general medical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1112-2016·2016-04-27

    Materne Recalls GoGo squeeZ Applesauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ applesauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12x4, Apple/Pineapple Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1117-2016·2016-04-27

    Materne Recalls GoGo squeeZ Apple Sauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12x4, Apple/Mixed Berry/Carrot (Boulder Berry) Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1095-2016·2016-04-27

    Centro Naturista Recalls Smart Lipo Dietary Supplement Capsules

    Centro Naturista is recalling Smart Lipo dietary supplements due to multiple regulatory violations. Consumers should stop using the product.

    Product
    Smart Lipo Dietary Supplement capsules, 950 mg, packaged in 30-count plastic bottle, Distributed by: SmartLipo365, Arlington, TX 76011
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1105-2016·2016-04-27

    Materne Recalls GoGo squeeZ Applesauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ applesauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12 x4, Apple/Pear Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1109-2016·2016-04-27

    Materne Recalls GoGo squeeZ Applesauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ applesauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 4x18, Apple/Berry Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1501-2016·2016-04-27

    Medtronic Recalls CareLink iPro2 Reports Due to Time Zone Error

    Medtronic MiniMed is recalling 19 CareLink iPro Therapy Management reports because they used the wrong time zone, causing inaccurate timestamps for continuous glucose data.

    Product
    CareLink iPro2 Reports, Model No. MMT-7340 is software intended to retrospectively calibrates sensor data and provides reports of continuous glucose information
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1524-2016·2016-04-27

    Synthes Recalls Cervical Spine Screws Due to Lot Swapping Error

    Synthes (USA) Products LLC is voluntarily recalling specific lots of cervical spine screws because two different screw types were swapped during manufacturing.

    Product
    Cervical Spine Locking Plate (CSLP) System, 4mm Cancellous Self Tapping Screw, Length 16mm Lot # 9666776 and 4mm Cortex Standard Screw, Length 16mm Lot # 9671879
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1104-2016·2016-04-27

    Materne Recalls GoGo squeeZ Apple Sauce Pouches for Potential Adulteration

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12 x4, 6 x12, 1 x 18, 1 x 48, 1 x100, 36 x 4, Mighty Mango Fruit & Veggies on the Go, (Apple/Mango/ButternutSquash) Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1119-2016·2016-04-27

    Materne Recalls GoGo squeeZ Applesauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ applesauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12x4, Apple/Yellow Carrot/Banana (Boatin' Banana) Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0827-2016·2016-04-27

    Hospira Recalls Dextrose Injection Bags Due to Chemical Contamination Risk

    Hospira is recalling 11,256 bags of Dextrose Injection, USP, 70% due to potential contamination with an aromatic hydrocarbon resin.

    Product
    Dextrose Injection, USP, 70%, Packaged as 500 mL in 1000 mL Bag, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7918-19, Barcode (01) 0 030409 791819 5
    Category
    Drug
    Distribution
    Distributed nationwide