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Medline Industries, Inc. DYNJAPF6057ARecalls & reported problems

Medline Industries, Inc. · ANESTHESIA CIRCUIT PEDS UNI-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 10889942976577), received between Oct 10, 2019 and Oct 10, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (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

  • Loss of or Failure to Bond1

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.

  • MalfunctionOct 10, 2019Loss of or Failure to Bond

    IT WAS REPORTED THAT THE ANESTHESIA CIRCUIT WAS NOT BONDED LEADING TO INACCURATE CO2 LEVELS DURING A PROCEDURE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9174788 ↗

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

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Sources and updates

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