Device recall
Z-0804-2019: Richard Wolf Bronchoscope Tubes, Model Texas. Device is reusable and should be…
FDA device recall · Class II · Richard Wolf GmbH
Key facts
| Recall number (Z-number) | Z-0804-2019 |
|---|---|
| Recall event | 81169 |
| Product | Richard Wolf Bronchoscope Tubes, Model Texas. Device is reusable and should be sterilized prior to each use. Product Usage: Bronchoscopes are intended for investigation, diagnosis and therapy of pathological changes and removal of foreign bodies in the area of the tracheobronchial respiratory… |
| Product code | KTI |
| Recalling firm | Richard Wolf GmbH |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3002808001 |
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