Device recall
Z-0717-2012: Model 750 24' MRI Reusable/Disposable Circuit Accessory for use with Model 750…
FDA device recall · Class II · Impact Instrumentation, Inc.
Key facts
| Recall number (Z-number) | Z-0717-2012 |
|---|---|
| Recall event | 60767 |
| Product | Model 750 24' MRI Reusable/Disposable Circuit Accessory for use with Model 750 Portable Ventilator |
| Product code | CAI |
| Recalling firm | Impact Instrumentation, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 11, 2013 |
| FEI number | 1220908 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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