Device recall
Z-0526-2014: Intubation Flexible Fiberscope, Models: 11301AA1, 11301BN1, 11302BD1, 11302BD2…
FDA device recall · Class II · Karl Storz Endoscopy America Inc
Key facts
| Recall number (Z-number) | Z-0526-2014 |
|---|---|
| Recall event | 66862 |
| Product | Intubation Flexible Fiberscope, Models: 11301AA1, 11301BN1, 11302BD1, 11302BD2, 11304BC1, 11340BC1, 11301BND1, 11302BDD1, and 11302BDD2. " Transoral intubation " Transnasal intubation " Evaluation of placement of endotracheal and double lumen endotracheal tubes " Provide visual access to the larynx… |
| Product code | CAL |
| Recalling firm | Karl Storz Endoscopy America Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 27, 2014 |
| FEI number | 2020550 |
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