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Zyno FE01Recalls & reported problems

Zyno Medical LLC · Extension Set: 10" In-Line .22 Micron Filter, Slide Clamp. Extension Sets are single-use IV administration sets for use with Z-800, Z-800F, Z-800W and Z-800WF Zyno Medical Infusion pumps. All extension sets fluid paths are sterile, non-Pyrogenic are not made with natural rubber latex, and are not made with DEHP. · 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 00814371020365), received between Jan 17, 2017 and Jan 17, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Operates Differently Than Expected” (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

  • Device Operates Differently Than Expected1

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.

  • MalfunctionJan 17, 2017Device Operates Differently Than Expected; Device Operates Differently Than Expected

    THIS IS A FOLLOW-UP FOR THE INITIALLY FILED MDR (3006575795-2017-00018).

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6258314 ↗

Other Set, Administration, Intravascular devices

All Set, Administration, Intravascular devices →

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