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