Device recall
Z-0340-2012: Infa Warmer i (Atom Infant Warmer Model 103) Atom Medical Corporation 3-18-15…
FDA device recall · Class II · Atom Medical Corporation
Key facts
| Recall number (Z-number) | Z-0340-2012 |
|---|---|
| Recall event | 59767 |
| Product | Infa Warmer i (Atom Infant Warmer Model 103) Atom Medical Corporation 3-18-15 Hongo, Bunkyo-Ku, Tokyo, Japan 113-0033 Usage: A warmer for infants. |
| Product code | FMZ |
| Recalling firm | Atom Medical Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 9, 2013 |
| 510(k) numbers | K102226 |
| FEI number | 3005652389 |
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