Medline Industries, Inc. DYNJAA10929Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10193489947083), received between Sep 29, 2026 and Sep 29, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Gas/Air Leak” (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

Recent adverse event reports

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

• MalfunctionSep 29, 2026Gas/Air Leak

  This VMSR report summarizes 2 malfunction events that occurred during Q1 2024 (January 1, 2024 through March 31, 2024). The account reported that DYNJAA10929 anesthesia circuits were leaking during use. The reported issue involved devices from Lot Numbers 23LB0579 and 23JBY286. The customer identified leaking circuits and arranged for multiple samples to be returned for evaluation, including one case containing eight units and an additional case from a second location. Photographs documenting the reported condition were provided, and samples were returned for investigation. No patient age, weight, sex, race, or ethnicity information was available. No patient or user injuries were reported.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50935176 ↗