Device recall
Z-2038-2009: First Responder Kit containing a 240-liter aluminum oxygen cylinder with…
FDA device recall · Class II · Allied Healthcare Products Inc
Key facts
| Recall number (Z-number) | Z-2038-2009 |
|---|---|
| Recall event | 52383 |
| Product | First Responder Kit containing a 240-liter aluminum oxygen cylinder with individually packaged regulator, cannula, and bag mask resuscitator, all packaged in a shipping container labeled as: Product #L903, Desc FIRST RESPONDER KIT, Catalog #L903. The brand and firm name on the label affixed to the… |
| Product code | ECX |
| Recalling firm | Allied Healthcare Products Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 23, 2012 |
| FEI number | 1924066 |
At a glance
- None 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