Device recall
Z-1225-06: Green Spec Fiberoptic Laryngoscope Handle - Stubby/Short; a battery operated…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-1225-06 |
|---|---|
| Recall event | 35669 |
| Product | Green Spec Fiberoptic Laryngoscope Handle - Stubby/Short; a battery operated fiberoptic laryngoscope handle for use with green coded fiberoptic systems and single use laryngoscope blades; Teleflex Medical, Bannockburn, IL 60015; catalog number 004413300 |
| Product code | CCW |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 28, 2009 |
| 510(k) numbers | K883414 |
| FEI number | 3004959265 |
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