Device recall
Z-0177-2013: Ventlab Premium Small Child Resuscitator, Manufactured by: Ventlab Corporation…
FDA device recall · Class I · Ventlab Corporation
Key facts
| Recall number (Z-number) | Z-0177-2013 |
|---|---|
| Recall event | 63347 |
| Product | Ventlab Premium Small Child Resuscitator, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028. |
| Product code | BTM |
| Recalling firm | Ventlab Corporation |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 30, 2013 |
| 510(k) numbers | K012842 |
| FEI number | 1314417 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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