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MEDLINE MDS600GORecalls & reported problems

Medline Industries, Inc. · PORTABLE DVT PUMP/SLEEVE,CORDLESS,10PR · Class 2

Adverse event reports
14
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 14 adverse event reports that list this exact device (DI 10197344098415), received between May 7, 2026 and Sep 30, 2026 — classified as 14 malfunctions.

The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (2 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 5 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 9 reportsOct 2026: 0 reports2024202520269
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Electrical /Electronic Property Problem2
  • Failure to Charge2
  • Aborted Charge1
  • Audible Prompt/Feedback Problem1
  • Battery Problem1
  • Display or Visual Feedback Problem1
  • Failure to Cycle1
  • Failure to Power Up1

Patient problems

  • No Clinical Signs, Symptoms or Conditions10
  • Insufficient Information4

Recent adverse event reports

The 14 most recent of 14 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 30, 2026Audible Prompt/Feedback Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50954115 ↗
  • MalfunctionSep 30, 2026Electrical /Electronic Property Problem

    It was reported that THIS IS THROWING A CODE AND NOT WOKRING.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50947970 ↗
  • MalfunctionSep 29, 2026Electrical /Electronic Property Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50935066 ↗
  • MalfunctionSep 28, 2026Premature Discharge of Battery

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50918240 ↗
  • MalfunctionSep 25, 2026Failure to Cycle

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50904108 ↗
  • MalfunctionSep 18, 2026Display or Visual Feedback Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50821922 ↗
  • MalfunctionSep 17, 2026Material Puncture/Hole; Gas/Air Leak

    It was reported that "ITEM WILL WORK AND THEN STOP AFTER ABOUT 5 COMPRESSIONS AND CONTINUOSLY BEEPS."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50805513 ↗
  • MalfunctionSep 16, 2026Failure to Power Up; Battery Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50789688 ↗
  • MalfunctionSep 14, 2026Power Problem

    It was reported that "This pump will not stay on."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50753804 ↗
  • MalfunctionMay 24, 2026Aborted Charge

    IT WAS REPORTED THAT CUSTOMER PUMP WAS CHARGING ALL WEEKEND AND LOST CHARGE WITHIN AN HOUR OF BEING APPLIED TO THE PATIENT.

    Patient problems: Insufficient Information

    MAUDE report 25266397 ↗
  • MalfunctionMay 22, 2026Unintended Power Up; Failure to Pump; Failure to Select Signal

    IT WAS REPORTED THAT ITEM IS NOT WORKING, BLINKING RED TO GREEN AND WILL NOT SHUT OFF; IT WON'T START OR STOP, DOESN'T PUMP UP.

    Patient problems: Insufficient Information

    MAUDE report 25262786 ↗
  • MalfunctionMay 21, 2026Failure to Charge

    IT WAS REPORTED THAT THE PUMP WAS CHARGING ALL WEEKEND AND LOST CHARGE WITHIN AN HOUR OF BEING APPLIED TO THE PATIENT.

    Patient problems: Insufficient Information

    MAUDE report 25249374 ↗
  • MalfunctionMay 12, 2026Failure to Charge

    CLIENT REPORTS, UNIT NOT HOLDING A CHARGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25153046 ↗
  • MalfunctionMay 7, 2026Inflation Problem

    PER PHONE CALL: CUSTOMER RECEIVED THIS UNIT FROM HER DRS OFFICE IN FEBRUARY, AND SHE IS NOT GETTING ANY RESULTS.

    Patient problems: Insufficient Information

    MAUDE report 25118730 ↗

Other SLEEVE, LIMB, COMPRESSIBLE devices

All SLEEVE, LIMB, COMPRESSIBLE devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.