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
Recalls naming this device
- 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, ClassifiedMicrostream 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, ClassifiedMicrostream 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, ClassifiedMicrostream 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, ClassifiedMicrostream 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, ClassifiedMicrostream 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, ClassifiedMicrostream 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, ClassifiedMicrostream 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, ClassifiedMicrostream 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, ClassifiedMicrostream 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, ClassifiedMicrostream Instructions for Use and Part Number used with - Product Description, REF: Microstream Adv. Infant Intubated, PT00134354 - Microstream Advance Neonatal-Infant Intub
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.