Device recall
Z-1066-2019: BVI Visitec Soft Tip Cannula, 0.8MM.50 x 33mm (25G x 1.3 in). The BVI Soft Tip…
FDA device recall · Class II · Beaver Visitec
Key facts
| Recall number (Z-number) | Z-1066-2019 |
|---|---|
| Recall event | 81757 |
| Product | BVI Visitec Soft Tip Cannula, 0.8MM .50 x 33mm (25G x 1.3 in). The BVI Soft Tip Cannula is intended to irrigate and/or aspirate ophthalmic solutions and liquids in or out of the eye, and remove materials where appropriate (e.g. retinal, subretinal procedures). |
| Product code | HMX |
| Recalling firm | Beaver Visitec |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 1, 2020 |
| FEI number | 1211998 |
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