Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1382-2025 — Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Adv. Infant Intubated, PT00134354 - Microstream Advance Neonatal-Infant Intubated CO2 Filter Line 2m/6.5ft Extended Duration, QMVIIH

U.S. FDA — Device Enforcement · Israel · 2025-02-17 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1382-2025
Date of alert
2025-02-17
Country / jurisdiction
Israel
Risk level
Class II
Risk type
recall
Brand
Oridion Medical 1987 Ltd.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10884521762374
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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