[Recalled] 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 Respirato
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| 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 ventil |
|---|---|
| Brand / manufacturer | Carefusion 2200 Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1901-2012 |
| Country of notice | United States |
| Risk level | Class I |
| Hazard type | recall |
| Notice date | 29 May 2012 |
| EAN / barcode | 0000414257 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: 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.
This Class I recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).
Read the full official notice →
Related recalls from Carefusion 2200 Inc
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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