Device recall
Z-1664-2014: Visitec Anterior Chamber Cannula,.40x22mm (27Gx7/8in) REF 585006 Cannulae are…
FDA device recall · Class II · Beaver-Visitec International Inc.
Key facts
| Recall number (Z-number) | Z-1664-2014 |
|---|---|
| Recall event | 68281 |
| Product | Visitec Anterior Chamber Cannula, .40x22mm (27Gx7/8in) REF 585006 Cannulae are intended to irrigate and or aspirate ophthalmic solutions and liquids in or out of the eye, and remove materials where appropriate. These products are used in all sections of the eye. This cannula is a general use cannula… |
| Product code | HMX |
| Recalling firm | Beaver-Visitec International Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 5, 2014 |
| 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