Device recall
Z-0192-2024: EVIS EXERA III BRONCHOVIDEOSCOPE Model Numbers BF-1TH190, BF-H190, BF-Q190 and…
FDA device recall · Class I · Olympus Corporation of the Americas
Key facts
| Recall number (Z-number) | Z-0192-2024 |
|---|---|
| Recall event | 93052 |
| Product | EVIS EXERA III BRONCHOVIDEOSCOPE Model Numbers BF-1TH190, BF-H190, BF-Q190 and BRONCHOVIDEOSCOPE OLYMPUS BF-Q170 Model Number BF-Q170 |
| Product code | NWB |
| Recalling firm | Olympus Corporation of the Americas |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K121959 |
| FEI number | 2429304 |
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