Medline DYNJAAHME10Recalls & reported problems
Medline Industries, Inc. · EXCHANGER,HEAT/MOIST,SM,SAMPLE PORT · Class 2
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 10884389120477), received between Aug 13, 2020 and Aug 13, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 Dislodged or Dislocated1
- Migration or Expulsion of Device1
- Nonstandard Device1
Patient problems
- Airway Obstruction1
- Foreign Body In Patient1
- Respiratory Distress1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 13, 2020Migration or Expulsion of Device; Nonstandard Device; Device Dislodged or Dislocated; Device Dislodged or Dislocated
THE FACILITY REPORTED THAT SHORTLY AFTER PLACING THE PRODUCT ON THE PATIENT THE HME FILTER WAS FOUND LODGED IN THE T-PIECE OF THE INLINE SUCTION NEAR THE INNER CANNULA OF THE TRACH REQUIRING MANUAL REMOVAL.
Patient problems: Airway Obstruction; Foreign Body In Patient; Respiratory Distress
MAUDE report 10401970 ↗
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- VOCSN V+C+Pro, JapaneseVentec Life Systems, Inc. · Filter, Bacterial, Breathing-Circuit1 recall33 reports
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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