Device recall
Z-0343-2009: AMO Healon D Ophthalmic Viscosurgical Device, Product Code: 10204011, Lot…
FDA device recall · Class I · Advanced Medical Optics, Inc.
Key facts
| Recall number (Z-number) | Z-0343-2009 |
|---|---|
| Recall event | 50179 |
| Product | AMO Healon D Ophthalmic Viscosurgical Device, Product Code: 10204011, Lot Number: UD30654, 30 mg/mL fill size |
| Product code | LZP |
| Recalling firm | Advanced Medical Optics, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Feb 21, 2012 |
| PMA numbers | P880031 |
| FEI number | 3003843509 |
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