RecallRadar

FDA Device recall Z-1901-2012

AirLife Isothermal Breathing Circuit Accessory - Infant Patient Y Connector

On 2012-07-11 the FDA classified a Class I recall of AirLife Isothermal Breathing Circuit Accessory - Infant Patient Y Connector by Carefusion 2200, citing the Y adapter within the breathing circuit may spontaneously crack, causing a leak in the closed ventilation system. This leak could lead to a decrease in the tidal volume deliver….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1901-2012
ClassificationClass I
Statusterminated
Initiated2012-05-29
Published2012-07-11
Last updated2026-09-13 11:53 UTC
CompanyCarefusion 2200
DistributionUS

Product

AirLife Isothermal Breathing Circuit Accessory - Infant Patient Y Connector; an Rx device for single patient use; 30 connectors per box; CareFusion, 22745 Savi Ranch Parkway, Yorba Linda, CA 92887 USA, Made in Mexico Respiratory breathing circuits are used with a ventilator when mechanical ventilation is administered to a patient.

Reason

The Y adapter within the breathing circuit may spontaneously crack, causing a leak in the closed ventilation system. This leak could lead to a decrease in the tidal volume delivered to the ventilated patient.

Identifiers

code_info
product codes 5925-504 and 6603-504; includes all lot numbers of the affected product codes manufactured prior to Febru…product codes 5925-504 and 6603-504; includes all lot numbers of the affected product codes manufactured prior to February 3, 2012, lot #0000414257 and any lot numbers beginning with the letter Y.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1901-2012%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.