Device recall
Z-0787-2020: Superset with 22MM ID, Double Swivel Elbow 22MM OD/15MM ID and Bronchoscopy…
FDA device recall · Class II · Intersurgical Inc
Key facts
| Recall number (Z-number) | Z-0787-2020 |
|---|---|
| Recall event | 83527 |
| Product | Superset with 22MM ID, Double Swivel Elbow 22MM OD/15MM ID and Bronchoscopy Port, REF 3521000. Airway connector. |
| Product code | BZA |
| Recalling firm | Intersurgical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 15, 2020 |
| 510(k) numbers | K911421 |
| FEI number | 1000120301 |
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