RecallRadar

FDA Device recall Z-1382-2025

Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Adv

On 2025-03-26 the FDA classified a Class II recall of Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Adv by Oridion Medical 1987, citing 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 dis….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1382-2025
ClassificationClass II
Statusongoing
Initiated2025-02-17
Published2025-03-26
Last updated2026-09-13 11:57 UTC
CompanyOridion Medical 1987
DistributionUS

Product

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

Reason

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.

Identifiers

code_infoPart Number and Revision - REF/UDI-DI(Lot): PT00134354 Rev A- QMVIIH/10884521762374(C210314316, C211085494)

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1382-2025%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.