Device recall
Z-0851-2020: VitreQ 23G VFI Cannula-REF: CN23.D03 GTIN: 8719214221423
FDA device recall · Class II · Vitreq Bv
Key facts
| Recall number (Z-number) | Z-0851-2020 |
|---|---|
| Recall event | 84661 |
| Product | VitreQ 23G VFI Cannula-REF: CN23.D03 GTIN: 8719214221423 |
| Product code | HMX |
| Recalling firm | Vitreq Bv |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 9, 2020 |
| FEI number | 3012037425 |
At a glance
- None Linked 510(k)s
- 10–99 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