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Medline Industries, Inc. DYNJAAF6718Recalls & reported problems

Medline Industries, Inc. · ANESTHSIA CIRCUIT ADULT-LF · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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 10888277798694), received between Nov 26, 2018 and Nov 26, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Detachment of Device or Device Component1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionNov 26, 2018Detachment of Device or Device Component

    IT WAS REPORTED THAT DURING AN UNIDENTIFIED PROCEDURE, THE ANESTHESIA CIRCUIT DETACHED FROM THE VENTILATOR.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8103213 ↗

Other Circuit, breathing (w connector, adaptor, y piece) devices

All Circuit, breathing (w connector, adaptor, y piece) devices →

Sources and updates

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