Device recall
Z-0907-04: Surgical Tubing Pack, Model: AMO Prestige Pack, Product Code OPO40
FDA device recall · Class II · Allergan Medical Optics Inc
Key facts
| Recall number (Z-number) | Z-0907-04 |
|---|---|
| Recall event | 28904 |
| Product | Surgical Tubing Pack, Model: AMO Prestige Pack, Product Code OPO40 |
| Product code | HQC |
| Recalling firm | Allergan Medical Optics Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 4, 2004 |
| 510(k) numbers | K924235 |
| 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