The Recall Desk

State

Minnesota product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

56776–56800 of 81684

  • HighFDA (Devices)·Z-0320-2016·2015-12-02

    Philips HeartStart MRx Monitor/Defibrillator Recalled for Software Issue

    Philips is recalling HeartStart MRx Monitor/Defibrillators because a software issue may cause the automated Ready-For-Use test to stop in an abnormal state when the device is turned off.

    Product
    Philips HeartStart MRx Monitor/Defibrillator; M3535A, M3536A, M3536J, M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536M6. For use for the termination of ventricular tachycardia and ventricular fibrillation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0326-2016·2015-12-02

    NxStage System One S Cycler Recalled for Ultrafiltration Software Error

    NxStage Medical is recalling 323 System One S Cycler units due to a software error that may cause inaccurate fluid removal during hemodialysis.

    Product
    NxStage System One S Cycler (High Permeability Hemodialysis System) Model no. NX1000-5
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0387-2016·2015-12-02

    Qualgen Recalls Testosterone Pellets Due to Sterility Assurance Concerns

    Qualgen is recalling 10,885 vials of compounded Testosterone USP pellets nationwide due to deficient practices that may impact sterility assurance.

    Product
    Testosterone USP 99.5%, .5% Stearic Acid NF Pellets, 3 mL, one-count vials, 25 mg (NDC 69761-125-01), 37.5 mg (NDC 69761-137-01), 50 mg (NDC 69761-150-01), 87.5 mg (NDC: 69761-187-01), 100 mg (NDC 69761-110-01), 200 mg (NDC 69761-120-01), Rx only, Compounded by Qualgen, Edmond…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0333-2016·2015-12-02

    Palindrome Precision Chronic Catheter Kit Recalled for Packaging Defect

    Covidien LLC is recalling 10 units of Palindrome Precision Chronic Catheter Kits due to incorrect packaging with a 90-degree bend at the distal tip.

    Product
    Palindrome Precision Chronic Catheter Kit Symmetrical Tip, Pre-Curved Shaft and Tal VenaTrac" Stylet 14.5 Fr/Ch (4.8mm) X 33 cm Item Number: 8888145061P The Palindrome chronic catheter is intended for acute and chronic hemodialysis, apheresis, and infusion. It may be…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0338-2016·2015-12-02

    Masimo Recalls Rainbow Reusable Sensors Due to Inaccurate Readings

    Masimo is recalling Rainbow Reusable Sensors because incompatible configurations may cause no readings or inaccurate SpCO and SpMet results.

    Product
    rainbow Reusable Sensors. RAINBOW DCI-DC3, SpO2/SpCO/SpMet, Part No. 2201; RAINBOW DCI-dc8, SpO2/SpCO/SpMet, Part No. 2407; RAINBOW DCI, SpO2/SpCO/SpMet, Part No. 2696; RAINBOW DCIP, PED, SpO2/SpCO/SpMet, Part No. 2697. rainbow reusable sensors are indicated for spot check…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16049·2015-12-02

    Felt Recalls 2015 Mountain Bicycles with Carbon Fiber Seatposts

    Felt Bicycles is recalling 645 model year 2015 mountain bikes because the carbon fiber seatposts can crack and break, posing injury and fall hazards.

    Product
    Mountain Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0339-2016·2015-12-02

    Siemens Dimension Vista Magnesium Reagent Cartridge Recall for Low Results

    Siemens Healthcare Diagnostics is recalling 3,601 Dimension Vista magnesium reagent cartridges due to erroneous low results that may affect patient and quality control testing.

    Product
    Dimension Vista System (MG) ; Flex reagent cartridge Catalog number K3057, SMN 10445158. For the quantitative measurement of magnesium in human serum, plasma and urine on the Dimension Vista System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V813000·2015-12-02

    Ford Recalls 2013 Escape and 2013-2014 Focus ST for Wiring Defect

    Ford is recalling specific 2013 Escape and 2013-2014 Focus ST vehicles because engine wiring splices may send incorrect signals, causing hesitation or stalling.

    Product
    FORD — FORD FOCUS, ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0332-2016·2015-12-02

    Palindrome Precision Chronic Catheter Kit Recalled for Packaging Defect

    Covidien LLC is recalling 150 units of Palindrome Precision Chronic Catheter Kits due to incorrect packaging with a 90-degree bend at the distal tip.

    Product
    Palindrome Precision Chronic Catheter Kit Symmetrical Tip, Tal VenaTrac" Stylet 14.5 Fr/Ch (4.8mm) X 33 cm Item Number: 8888145046C The Palindrome chronic catheter is intended for acute and chronic hemodialysis, apheresis, and infusion. It may be inserted either…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0329-2016·2015-12-02

    Palindrome Chronic Catheter Kit Recalled for Packaging Defect

    Covidien LLC is recalling 280 units of Palindrome Chronic Catheter Kits because they were incorrectly packaged with a 90-degree bend at the distal tip.

    Product
    Palindrome" Chronic Catheter Kit Symmetrical Tip, Tal VenaTrac" Stylet 14.5 Fr/Ch (4.8mm) X 33 cm Item Number: 8888145042 The Palindrome chronic catheter is intended for acute and chronic hemodialysis, apheresis, and infusion. It may be inserted either percutaneously or by…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0330-2016·2015-12-02

    Palindrome Precision Chronic Catheter Kit Recalled for Packaging Defect

    Covidien LLC is recalling 160 units of Palindrome Precision Chronic Catheter Kits because they were incorrectly packaged with a 90-degree bend at the distal tip.

    Product
    Palindrome Precision Chronic Catheter Kit Symmetrical Tip 14.5 Fr/Ch (4.8mm) X 33 cm Item Number: 8888145017P The Palindrome chronic catheter is intended for acute and chronic hemodialysis, apheresis, and infusion. It may be inserted either percutaneously or by cutdown.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0341-2016·2015-12-02

    Leica Microsystems Recalls Unstable CD10 Monoclonal Antibody Diagnostic Reagents

    Leica Microsystems is recalling specific lots of Novocastra CD10 antibody reagents because they are not stable up to the labeled expiry date.

    Product
    Novocastra Lyophilized Mouse Monoclonal Antibody CD10 (CD10). Immunohistochemistry. in vitro diagnostic. 0.1ml NCL-CD10-270 and 1mL NCL-CD10-270 are intended for the qualitative identification by light microscopy of CD10 molecules in paraffin sections.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0325-2016·2015-12-02

    Philips MRI Systems Recalled for Reversed Image Order in MobiView Software

    Philips is recalling specific MRI systems with MobiView software due to a defect that reverses the order of fused multi-station scan images.

    Product
    Ingenia, Intera, Achieva and Achieve dStream MR systems on Software versions R5.1.7 and R5.1.8 with the Mobi View software option. Diagnostic imaging system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0328-2016·2015-12-02

    Biochemical Diagnostics Recalls hCG Control Kits Due to Labeling Discrepancies

    Biochemical Diagnostics Inc. is recalling CONSULT hCG Controls Kits because storage temperature instructions on the kit labels do not match the vial labels and package insert.

    Product
    CONSULT(TM) diagnostics hCG CONTROLS Kit, Part/Reorder Number 5011, IVD Product Usage - CONSULT Diagnostics hCG Controls are intended to validate the performance of qualitative hCG urine procedures and immunochromatographic devices.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0323-2016·2015-12-02

    Synthes 2.4mm Locking Screws Recalled for Incorrect Package Insert

    Synthes (USA) Products LLC is recalling 229 units of 2.4mm Locking Screws because they may contain the wrong package insert.

    Product
    2.4MM locking screw SLF-TPNG with Stardrive Recess 18 mm. Intended for fixation of fractures, osteotomies, nonunions, replantations, and fusions of small bones and small bone fragments, particularly in osteopenic bone.
    Category
    Medical Device
    Distribution
    27 states
  • HighNHTSA·15V808000·2015-12-01

    Newmar Recalls Motorhomes Due to Refrigerator Door Latch Defect

    Newmar is recalling specific motorhomes because refrigerator door latches may lock without the operator's knowledge, posing a risk of injury if a person is trapped inside.

    Product
    NEWMAR — NEWMAR VENTANA, VENTANA LE, CANYON STAR, DUTCH STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V810000·2015-12-01

    Altec Recalls 2011-2015 Brush Chippers Due to Weld Defects

    Altec is recalling 2011-2015 DSC6 and DC610 brush chippers because improper welds or incorrect spacers may cause the anvil to detach, posing an injury risk.

    Product
    ALTEC — ALTEC DSC6 BRUSH CHIPPER, DC610 BRUSH CHIPPER
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V802000·2015-11-30

    Yamaha Recalls 2015 YZF-R1 Motorcycles Due to Transmission Gear Failure

    Yamaha is recalling 2,921 model year 2015 YZF-R1 motorcycles because transmission gears may fail, potentially causing the transmission to lock up and increasing the risk of a crash.

    Product
    YAMAHA — YAMAHA YZFR1MF, YZFR1MFC, YZFR1, YZFR1C
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V803000·2015-11-30

    Newmar Recalls 2014-2015 Motorhomes Due to Cargo Door Lock Fire Risk

    Newmar is recalling specific 2014-2015 motorhomes because cargo door lock actuators may overheat and melt, increasing the risk of a fire.

    Product
    NEWMAR — NEWMAR MOUNTAIN AIRE, VENTANA, ESSEX, DUTCH STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V804000·2015-11-30

    Mack Trucks Recalls 2010-2016 Granite Trucks Due to Brake Imbalance

    Mack Trucks is recalling 2010-2016 Granite 4X2 trucks because a brake imbalance may cause rear brakes to overheat, increasing the risk of tire blowouts or wheel-end fires.

    Product
    MACK — MACK GRANITE (GU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V805000·2015-11-30

    Terex Environmental Recalls Wood Chippers Due to Decal Adhesion Issues

    Terex Environmental is recalling 2007-2015 wood chippers because safety decals may detach, increasing injury risk.

    Product
    TEREX ENVIRONMENTAL — TEREX ENVIRONMENTAL MODEL 720 WOOD CHIPPER, MODEL 700 WOOD CHIPPER, MODEL 750 WOOD CHIPPER, MODEL 705 WOOD CHIPPER
    Category
    Vehicle
    Distribution
    Distributed nationwide