Device recall
Z-0110-2012: Mask adult, oxygen, high concentration, non-rebreathing, elastic strap style…
FDA device recall · Class II · Salter Laboratories, Division of Regulatory Affairs
Key facts
| Recall number (Z-number) | Z-0110-2012 |
|---|---|
| Recall event | 58454 |
| Product | Mask adult, oxygen, high concentration, non-rebreathing, elastic strap style, w/9' tube and safety vent - 50/cs; Mask adult, oxygen, high concentration, non-rebreathing, elastic strap style, w safety vent - 50/cs; Mask adult, oxygen, high concentration, non-rebreathing, elastic strap style, w/7'… |
| Product code | BYG |
| Recalling firm | Salter Laboratories, Division of Regulatory Affairs |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 26, 2011 |
| FEI number | 1314417 |
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