Device recall
Z-0758-2007: Conditional Fiber Optic Laryngoscope Kit, which contains laryngoscope blades…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-0758-2007 |
|---|---|
| Recall event | 37591 |
| Product | Conditional Fiber Optic Laryngoscope Kit, which contains laryngoscope blades, handles and 2 battery packs for use in Magnetic Resonance environments; Distributed by Teleflex Medical, Research Triangle Park, NC 27709; catalog number 005852300 |
| Product code | CCW |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 3, 2007 |
| 510(k) numbers | K062523 |
| 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