Device recall
Z-0485-2007: Fisher & Paykel IW930 CosyCot Infant Radiant Warmer (with integrated bed) fitted…
FDA device recall · Class II · Fisher & Paykel Healthcare Ltd
Key facts
| Recall number (Z-number) | Z-0485-2007 |
|---|---|
| Recall event | 37003 |
| Product | Fisher & Paykel IW930 CosyCot Infant Radiant Warmer (with integrated bed) fitted with 9001W005J Elevator Module |
| Product code | FMT |
| Recalling firm | Fisher & Paykel Healthcare Ltd |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 26, 2012 |
| 510(k) numbers | K970432 |
| FEI number | 3002806988 |
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