Hemo-Force MDS600INT2Recalls & reported problems
Medline Industries, Inc. · PUMP,MEDLINE,DVT,INTERMITTENT,GEN2 · Class 2
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10888277348097), received between Sep 19, 2026 and Sep 29, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Break” (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
- Break1
- Crack1
- Electrical /Electronic Property Problem1
- Failure to Charge1
- Failure to Power Up1
- Insufficient Cooling1
- Material Discolored1
- Pressure Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- 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 29, 2026Failure to Charge; Pressure Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50940809 ↗MalfunctionSep 29, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50933811 ↗MalfunctionSep 28, 2026Insufficient Cooling; Crack
It was reported that "THE RIGHT SIDE DOES NOT INFLATE AND WHERE THE HOSE CONNECTS TO THE SCD IS CRACKED".
Patient problems: Insufficient Information
MAUDE report 50913234 ↗MalfunctionSep 19, 2026Break; Material Discolored; Failure to Power Up
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50831741 ↗
Other SLEEVE, LIMB, COMPRESSIBLE devices
- Kendall 84021Cardinal Health 200, LLC · SLEEVE, LIMB, COMPRESSIBLE2 recalls0 reports
- Kendall SCD 29525Cardinal Health, Inc. · Sleeve, Limb, Compressible56 reports
- RAW MATERIAL 30MDjo, LLC · SLEEVE, LIMB, COMPRESSIBLE52 reports
- Kendall 84021BCardinal Health 200, LLC · SLEEVE, LIMB, COMPRESSIBLE1 recall0 reports
- AIRCAST 3011-PLDjo, LLC · SLEEVE, LIMB, COMPRESSIBLE1 recall0 reports
- Kendall 84021PCardinal Health 200, LLC · SLEEVE, LIMB, COMPRESSIBLE1 recall0 reports
- N/AStryker Sustainability Solutions, Inc. · SLEEVE, LIMB, COMPRESSIBLE1 recall0 reports
- N/AStryker Sustainability Solutions, Inc. · SLEEVE, LIMB, COMPRESSIBLE1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.