Device recall
Z-1900-2012: AirLife Isothermal Breathing Circuit, Infant Respiratory Circuit, Non-Heated; an…
FDA device recall · Class I · Carefusion 2200 Inc
Key facts
| Recall number (Z-number) | Z-1900-2012 |
|---|---|
| Recall event | 61943 |
| Product | AirLife Isothermal Breathing Circuit, Infant Respiratory Circuit, Non-Heated; an Rx device for single patient use; 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… |
| Product code | BZE |
| Recalling firm | Carefusion 2200 Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jan 22, 2016 |
| 510(k) numbers | K915226 |
| FEI number | 3008002452 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database