Microstream Advance MVABO100URecalls & reported problems
Oridion Medical 1987 Ltd. · Adult-Intermediate Bite Block CO2 Filter Line with O2 Tubing; Short-term use: Procedural/Emergency · Class 2
All models of Microstream Advance (13)
Data updated Oct 16, 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 20884521761749), received between Mar 15, 2023 and Mar 15, 2023 — classified as 1 malfunction.
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 16, 2026.
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available1
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 15, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE REPORTER, DURING A PROCEDURE, THE PATIENT COUGHED BLOOD AND IT ENTERED THE CAPNOGRAPHY LINE. THE RESPIRATORY THERAPIST WAS QUICK TO DISCONNECT THE ETCO2 LINE FROM THE CAPNOGRAPH SO IT WOULD NOT BE CONTAMINATED. THE BLOOD FROM THE PATIENT CAUSED THE CAPNOGRAPHY LINE TO STOP WORKING PROPERLY.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 16550190 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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