Hemo-Force MDS600INTRecalls & reported problems
Medline Industries, Inc. · PUMP,MEDLINE,DVT,INTERMITTENT,SPRG HOOKS · Class 2
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 40884389817910), received between Nov 6, 2024 and Sep 28, 2026 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Incomplete or Inadequate Connection” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Incomplete or Inadequate Connection1
- Power Problem1
- Sparking1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 28, 2026Power Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50926363 ↗MalfunctionSep 14, 2026Incomplete or Inadequate Connection
It was reported that PUMP Will not turn on.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50759410 ↗InjuryNov 6, 2024Sparking; Sparking
ACCORDING TO THE FACILITY ON (B)(6), "STAFF COULD NOT POWER ON THE UNIT AND SUBMITTED IT TO US IN BIOMED."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20624831 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.