Device recall
Z-0553-05: RT130 and RT131 Neonatal/ Infant Breathing Circuits, heated wire. For use with…
FDA device recall · Class II · Fisher & Paykel Healthcare Inc
Key facts
| Recall number (Z-number) | Z-0553-05 |
|---|---|
| Recall event | 31046 |
| Product | RT130 and RT131 Neonatal/ Infant Breathing Circuits, heated wire. For use with MR850 Respiratory Humidifier. |
| Product code | BTT |
| Recalling firm | Fisher & Paykel Healthcare Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 21, 2005 |
| 510(k) numbers | K020332 |
| 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