Medline Industries, Inc. DYNJAA10312CRecalls & reported problems
Medline Industries, Inc. · ANES CIRCUIT 90IN ADULT EXP-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 10193489274929), received between Oct 31, 2025 and Oct 31, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Failure to Seal” (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.
Reports received per month
Most reported problems
Device problems
- Failure to Seal1
- Material Twisted/Bent1
- Mechanical Problem1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 31, 2025Mechanical Problem; Material Twisted/Bent; Failure to Seal; Mechanical Problem; Material Twisted/Bent; Failure to Seal
ACCORDING TO THE FACILITY, THE "WE ARE SEEING QUITE A FEW OF THE MASKS IN THE ANESTHESIA KITS THAT ARE BENT AT THE CONNECTION OF THE TUBING AND THE MASK. THIS IS NOT ALLOWING FOR A SEAL WHEN BEING USED."
Patient problems: Insufficient Information
MAUDE report 23441813 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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