Device recall
Z-0870-2012: Model 73X Uni-Vent Product Usage: Intended for use at mass casualty incidents.
FDA device recall · Class II · Impact Instrumentation, Inc.
Key facts
| Recall number (Z-number) | Z-0870-2012 |
|---|---|
| Recall event | 60786 |
| Product | Model 73X Uni-Vent Product Usage: Intended for use at mass casualty incidents. |
| Product code | BTL |
| Recalling firm | Impact Instrumentation, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 23, 2013 |
| 510(k) numbers | K051476 |
| FEI number | 1220908 |
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