MEDLINE DYNJAAMASK36Recalls & reported problems
Medline Industries, Inc. · MASK,FLEXIBLE,ANESTH,SIZE 6,TOP VALVE · Class 1
- 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 10888277399327), received between Sep 30, 2026 and Sep 30, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Deformation” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Material Deformation1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Material Deformation
It was reported that "This mask is sporadically coming in the packs defected."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50945212 ↗
Other MASK, GAS, ANESTHETIC devices
- Ventlab BT4040Ventlab, LLC · Mask, Gas, Anesthetic1 recall0 reports
- Ventlab BT2048Ventlab, LLC · Mask, Gas, Anesthetic1 recall0 reports
- Ventlab BT4018Ventlab, LLC · Mask, Gas, Anesthetic1 recall0 reports
- Ventlab BT4013Ventlab, LLC · Mask, Gas, Anesthetic1 recall0 reports
- Ventlab BT4019Ventlab, LLC · Mask, Gas, Anesthetic1 recall0 reports
- Ventlab BT4022Ventlab, LLC · Mask, Gas, Anesthetic1 recall0 reports
- Ventlab BT4015Ventlab, LLC · Mask, Gas, Anesthetic1 recall0 reports
- Ventlab BT4024Ventlab, LLC · Mask, Gas, Anesthetic1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.