Medline MDS600SQ2Recalls & reported problems
Medline Industries, Inc. · PUMP,MEDLINE,DVT,SEQUENTIAL, GEN2 · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10888277348103), received between Nov 16, 2023 and Sep 17, 2026 — classified as 1 injury, 3 malfunctions.
The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (1 report).
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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Electrical /Electronic Property Problem1
- Failure to Power Up1
- Insufficient Device Problem Information1
- Temperature Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Electric Shock1
- Insufficient Information1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 17, 2026Failure to Power Up
It was reported that "WONT POWER ON UNIT HAS BEEN TESTED ON MULTIPLE OUTLETS".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50797437 ↗MalfunctionSep 15, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50778750 ↗InjuryFeb 7, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
ACCORDING TO THE FACILITY, THE DEVICE ALLEGEDLY SHOCKED THE NURSE.
Patient problems: Electric Shock
MAUDE report 21337442 ↗MalfunctionNov 16, 2023Temperature Problem; Temperature Problem
"INTERNAL FIRE / EXPLOSION CAUSED DAMAGE TO ALL COMPONENTS".
Patient problems: Insufficient Information
MAUDE report 18148258 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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