Device recall
Z-0344-2007: COMPLETE MoisturePLUS Multi-Purpose Solution (US and Asia Pacific markets…
FDA device recall · Class II · Advanced Medical Optics, Inc.
Key facts
| Recall number (Z-number) | Z-0344-2007 |
|---|---|
| Recall event | 36711 |
| Product | COMPLETE MoisturePLUS Multi-Purpose Solution (US and Asia Pacific markets, excluding Japan) & COMPLETE Amino Moist Multi-Purpose Solution (Japan only) |
| Product code | LPN |
| Recalling firm | Advanced Medical Optics, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 17, 2010 |
| 510(k) numbers | K023226 |
| FEI number | 3003843509 |
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