Device recall
Z-1575-05: Lasik Custom Pak containing 1 dual tip irrigator, 8 ports, 16 G, 2 packs spears…
FDA device recall · Class II · Alcon Research, Ltd
Key facts
| Recall number (Z-number) | Z-1575-05 |
|---|---|
| Recall event | 33409 |
| Product | Lasik Custom Pak containing 1 dual tip irrigator, 8 ports, 16 G, 2 packs spears, eye, ocucel, 5S, PVA, 1 cover, support, tray 2.2MIL 6FD, and 2 dressings, tegaderm, 2 3/8 x 2 3/4. All contents considered sterile unless package is opened or damaged.RX Only. Part number 10162-01. (The Vidaurri LASIK… |
| Product code | LQJ |
| Recalling firm | Alcon Research, Ltd |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 20, 2007 |
| FEI number | 1610287 |
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