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Medline Industries, Inc. DYNJAP9908Recalls & reported problems

Medline Industries, Inc. · ANESTHESIA CIRCUIT PEDS-LF · Class 1

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

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10889942258079), received between Jun 26, 2019 and Jun 26, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Difficult to Insert” (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

  • Difficult to Insert1

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.

  • InjuryJun 26, 2019Difficult to Insert

    IT WAS REPORTED THAT THE ANESTHESIOLOGIST WAS UNABLE TO PUT THE CAP ON THE VALVE DURING PATIENT TRANSPORT RESULTING IN THE PATIENT EXPERIENCING DESATURATION.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8735518 ↗

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Sources and updates

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