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VasoPress VP520LRecalls & reported problems

Compression Therapy Concepts, Inc. · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00815245010581), received between Oct 16, 2017 and Oct 16, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Component Falling” (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.

Most reported problems

Device problems

  • Component Falling1
  • Detachment Of Device Component1
  • Loose or Intermittent Connection1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionOct 16, 2017Detachment Of Device Component; Component Falling; Loose or Intermittent Connection

    AIR TUBE IS LOOSE AND FALLS OUT OF FOOT SLEEVE WHEN PATIENT MOVES THEIR FOOT OR DEVICE IS TURNED ON. SEVERAL OF THE FOOT SLEEVES HAVE BEEN FOUND WITH LOOSE TUBES CAUSING THIS ISSUE MULTIPLE TIMES. THIS DEFECT RENDERS THE FOOT SLEEVE UNUSABLE AND STAFF HAS TO OPEN MULTIPLE PACKAGES TO FIND FOOT SLEEVES WITH SECURE TUBING.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6951581 ↗

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.