Oridion Medical recalls Microstream CO2 filter lines for adult-pediatric use due to risk of treatment delay or unintended extubation during procedures like suctioning, potentially causing respiratory failure.
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.
Oridion Medical is recalling Microstream CO2 filter lines for adult and pediatric patients. These devices may cause treatment delays or unintended extubation during procedures like suctioning, which could lead to respiratory failure or other serious complications.
The CO2 filter line may not disconnect properly from the endotracheal tube during procedures like suctioning. This can cause treatment delays or unintended extubation, leading to respiratory failure, low oxygen levels, or aspiration.
Healthcare providers using the Microstream CO2 filter lines for intubated patients in hospitals or clinics are most at risk. Patients receiving mechanical ventilation with this equipment could experience complications during medical procedures.
Check for the part number PT00134333 with revision A on the Microstream CO2 filter line. These lines were sold for short-term procedural use (QMVAI) or extended duration (QMVAIH) in hospitals and clinics.
Look for part number PT00134333 with revision A on the Microstream CO2 filter line.
Reach out to Oridion Medical for guidance on next steps if you have the recalled product.
The Microstream CO2 filter line may not disconnect properly from the endotracheal tube during procedures like suctioning, which can cause treatment delays or unintended extubation.
Using the recalled Microstream CO2 filter line may lead to treatment delays, unintended extubation, respiratory failure, hypoxia, or aspiration.
Check for part number PT00134333 with revision A on the Microstream CO2 filter line, which was sold for short-term procedural use (QMVAI) or extended duration (QMVAIH).
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1381-2025 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-1381-2025 from Oridion Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
