Device recall
Z-0044-2017: Willy Rusch GmbH Tracheostomy Tube Set Cannulation of tracheotomised patients…
FDA device recall · Class I · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-0044-2017 |
|---|---|
| Recall event | 75053 |
| Product | Willy Rusch GmbH Tracheostomy Tube Set Cannulation of tracheotomised patients, particularly in the case of a narrow tracheostoma and narrow-lumen tracheas. When using cannulas with curr. For short term intermittent inflation. |
| Product code | JOH |
| Recalling firm | Teleflex Medical |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 21, 2017 |
| 510(k) numbers | K964056 |
| FEI number | 3005747797 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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