Device recall
Z-1488-2012: BOMImed Reusable Integrated Fiber Optic Laryngoscope Blades, MacIntosh and…
FDA device recall · Class II · Bomimed Inc
Key facts
| Recall number (Z-number) | Z-1488-2012 |
|---|---|
| Recall event | 61464 |
| Product | BOMImed Reusable Integrated Fiber Optic Laryngoscope Blades, MacIntosh and Miller styles - all sizes. Instrument is used to aid with intubation. |
| Product code | EQN |
| Recalling firm | Bomimed Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 8, 2012 |
| FEI number | 3005396516 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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