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Medline Industries, Inc. DYNJAA9965DRecalls & reported problems

Medline Industries, Inc. · ANES CIRC ADULT 90IN EXP-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 10889942539192), received between Apr 23, 2018 and Apr 23, 2018 — 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Device Operates Differently Than Expected1
  • Moisture Damage1

Patient problems

  • Swelling1

Recent adverse event reports

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

  • MalfunctionApr 23, 2018Moisture Damage; Device Operates Differently Than Expected

    IT WAS REPORTED THAT MOISTURE IN THE FILTER WAS NOT ALLOWING THE PRESSURE TO RELEASE DURING A PROCEDURE.

    Patient problems: Swelling

    MAUDE report 7450744 ↗

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Sources and updates

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