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Microstream Advance MVAIHHRecalls & reported problems

Oridion Medical 1987 Ltd. · Adult-Pediatric Intubated CO2 Filter Line; High Humidity · Class 2

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20884521762005), received between May 7, 2025 and May 7, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Defective Component” (1 report).

1 FDA recall record name this device's identifier, 1 still open.

10 other recalls cover devices cleared under the same FDA submission (K181467); they may or may not involve this specific model.

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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 1 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Recalls naming this device

  1. Feb 17, 2025Open, Classified

    Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2 Oral-Nasal Filter Line/Intubated Filter (CO2) Line device users may experience difficulty/inability to disconnect adapter from endotracheal tube for procedures (e.g. suctioning), may cause treatment delay and/or unintended extubation, which could lead to respiratory failure, hypoxia, aspiration, and/or low oxygen saturation.

    Z-1384-2025 · Root cause: Labeling design · FDA record ↗

Most reported problems

Device problems

  • Defective Component1
  • Difficult or Delayed Separation1
  • Obstruction of Flow1

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.

  • MalfunctionMay 7, 2025Defective Component; Obstruction of Flow; Difficult or Delayed Separation; Defective Component; Obstruction of Flow; Difficult or Delayed Separation

    IT WAS REPORTED THAT THE DEVICE WAS ASSOCIATED WITH SHORTER LONGEVITY OF THE AIRWAY ADAPTER DUE TO PRESUMED MOISTURE OCCLUSION OF THE LINE, REQUIRING FREQUENT REPLACEMENT FOR MONITORING. ADDITIONALLY, DIFFICULTIES WERE NOTED IN PHYSICALLY DETACHING THE AIRWAY ADAPTER FROM THE CLOSED-SUCTION CATHETER SYSTEM. THE ISSUE WAS OBSERVED DURING USE. THERE WAS NO PATIENT INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21975945 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K181467. One submission often covers many models, so check the product and lot details in each record.

  • Z-1722-2025 · Apr 7, 2025 · Open, Classified
    Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pedi Intub CO2 Line STerm , Adt/Pedi Intub CO2 Line STerm Lng , Adt/Pedi Intub CO2 Line High Humidity
  • Z-1385-2025 · Feb 17, 2025 · Open, Classified
    Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Advance Intubated Infant, PT00156250 - Microstream Advance Neonatal-Infant In
  • Z-1376-2025 · Feb 17, 2025 · Open, Classified
    Microstream Instructions for Use and Part Number used with - Product Description, REF: FilterLine H Set & VitaLine H Set Infant/Neonatal, 006147 - MICROSTREAM FilterLine H Set I
  • Z-1378-2025 · Feb 17, 2025 · Open, Classified
    Microstream Instructions for Use and Part Number used with - Product Description, REF: Filter Line Sets Adult/Pediatric & Infant/Neonatal, 10129497 - CapnoLine Neonatal-Infant
  • Z-1380-2025 · Feb 17, 2025 · Open, Classified
    Microstream Instructions for Use and Part Number used with - Product Description, REF: OmniVentLine Set, 012808 - OmniVentLine Set Adult-Pediatric CO2 Sampling Line and Airway
  • Z-1383-2025 · Feb 17, 2025 · Open, Classified
    Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Luer Intubated Adult Pediatric, PT00156355 - Microstream Luer Adult-Pediatric
  • Z-1379-2025 · Feb 17, 2025 · Open, Classified
    Microstream Instructions for Use and Part Number used with - Product Description, REF: Airway Adapter and CO2 Sampling Line, 01158 - Microstream Luer Adult-Pediatric Airway Ada
  • Z-1381-2025 · Feb 17, 2025 · Open, Classified
    Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Adv. Adult-Pediatric Intubated, PT00134333 - Microstream Advance Adult-Pediat
  • Z-1377-2025 · Feb 17, 2025 · Open, Classified
    Microstream Instructions for Use and Part Number used with - Product Description, REF: FilterLine Sets & VitaLine Sets Adult/Pediatric, MQ04616 - MICROSTREAM FilterLine H Set L
  • Z-1382-2025 · Feb 17, 2025 · Open, Classified
    Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Adv. Infant Intubated, PT00134354 - Microstream Advance Neonatal-Infant Intub

Other ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE devices

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.