Oridion Medical recalls Microstream infant CO2 sampling lines due to risk of treatment delay during suctioning. Affected units may cause unintended extubation, respiratory failure, or hypoxia.
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.
Orid:ion Medical recalls infant CO2 sampling lines that may cause treatment delays during suctioning. If not properly disconnected, these lines could lead to respiratory failure, hypoxia, or aspiration.
The CO2 sampling line may not disconnect properly during suctioning procedures. This can cause treatment delays, unintended extubation, and potential respiratory failure, hypoxia, or aspiration.
Parents and caregivers of infants using this medical device for breathing support. Infants with respiratory conditions are at highest risk.
Check for the part number PT00134354 with revision A on the device. The product was sold as Microstream Advance Neonatal-Infant Intubated CO2 Filter Line 2m/6.5ft Extended Duration.
Look for part number PT00134354 with revision A on the device label.
The device may not disconnect properly during suctioning, causing treatment delays, unintended extubation, and potential respiratory failure, hypoxia, or aspiration.
Check for part number PT00134354 with revision A on the device label. The product was sold as Microstream Advance Neonatal-Infant Intubated CO2 Filter Line 2m/6.5ft Extended Duration.
The recall record does not specify a remedy or action steps for affected users.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1382-2025 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-1382-2025 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.
