Device recall
Z-0555-04: BE 183 Series Manual Jet Ventilators. Manual Jet Ventilator
FDA device recall · Class II · Instrumentation Industries Inc
Key facts
| Recall number (Z-number) | Z-0555-04 |
|---|---|
| Recall event | 27419 |
| Product | BE 183 Series Manual Jet Ventilators. Manual Jet Ventilator |
| Product code | BTM |
| Recalling firm | Instrumentation Industries Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 26, 2004 |
| 510(k) numbers | K991785 |
| FEI number | 2518436 |
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