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Medline Industries, Inc. DYNJAA9015Recalls & reported problems

Medline Industries, Inc. · ANES CIRC EXTENDAFLEX-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 10080196979226), received between Feb 26, 2021 and Feb 26, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “No Pressure” (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

  • No Pressure1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionFeb 26, 2021No Pressure

    IT WAS REPORTED LOSS OF PRESSURE IN VENTILATION OF PATIENT AFTER INTUBATION AND ANESTHESIA CIRCUIT HOOK-UP.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11388774 ↗

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Sources and updates

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