Device recall
Z-0414-2009: Fisher & Paykel Healthcare RT240 Adult Breathing Circuit Kit. lntended Use: The…
FDA device recall · Class II · Fisher & Paykel Healthcare Inc
Key facts
| Recall number (Z-number) | Z-0414-2009 |
|---|---|
| Recall event | 50105 |
| Product | Fisher & Paykel Healthcare RT240 Adult Breathing Circuit Kit. lntended Use: The dual heated adult respiratory ventilator circuits are intended as conduits of breathing gas for ventilation of patients, and to maintain the temperature of the humidified gas, to reduce condensation. |
| Product code | BTT |
| Recalling firm | Fisher & Paykel Healthcare Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 26, 2012 |
| 510(k) numbers | K983112 |
| FEI number | 3000210616 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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