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Liberty® 026-20226Recalls & reported problems

Fresenius Medical Care Holdings, Inc. · Liberty® Drain Set · Class 2

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00840861100620), received between Aug 7, 2017 and Aug 7, 2017 — classified as 1 death.

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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Death1

Recent adverse event reports

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

  • DeathAug 7, 2017Adverse Event Without Identified Device or Use Problem

    A PERITONEAL DIALYSIS PATIENT'S NURSE REPORTED THAT ON (B)(6) 2017, THE PATIENT CODED AND SUBSEQUENTLY EXPIRED ON A LIBERTY CYCLER. THERE IS NO TEMPORAL ASSOCIATION BETWEEN THE PATIENTS¿ DEATH AND LIBERTY CYCLER AND THE LIBERTY CYCLER SET. THERE IS CONFIRMED PATIENT COMPLETION OF THE CCPD TREATMENT. THERE IS NO DOCUMENTATION SUPPORTING A POSSIBLE ASSOCIATION BETWEEN THE LIBERTY CYCLER, THE LIBERTY CYCLER SET AND THE EXPIRATION OF THE PATIENT.

    Patient problems: Death

    MAUDE report 6772349 ↗

Other SYSTEM, PERITONEAL, AUTOMATIC DELIVERY devices

All SYSTEM, PERITONEAL, AUTOMATIC DELIVERY devices →

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