Device recall
Z-3238-2017: BOMImed Disposable Fiber Optic Medium Laryngoscope Handle. Each handle is…
FDA device recall · Class II · Bomimed
Key facts
| Recall number (Z-number) | Z-3238-2017 |
|---|---|
| Recall event | 77958 |
| Product | BOMImed Disposable Fiber Optic Medium Laryngoscope Handle. Each handle is packaged in an individual peel pouch, 20 handles per box. The rigid laryngoscope handle is a device used along with a blade to examine and visualize a patient's airway and aid placement of a tracheal tube. |
| Product code | CCW |
| Recalling firm | Bomimed |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 1, 2021 |
| FEI number | 3003213883 |
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