Device recall
Z-0408-2022: Malosa Core Phaco Pack 2- Medical Refractive Kit intended to be used to aid in…
FDA device recall · Class II · Beaver Visitec International, Inc.
Key facts
| Recall number (Z-number) | Z-0408-2022 |
|---|---|
| Recall event | 89111 |
| Product | Malosa Core Phaco Pack 2- Medical Refractive Kit intended to be used to aid in cataract, corneal, or refractive surgery. Part Number: MMK834/1 |
| Product code | PZG |
| Recalling firm | Beaver Visitec International, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1211998 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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