Device recall
Z-0642-2012: Neulook Fancy FX is packaged in a small glass bottle with a orange, white, and…
FDA device recall · Class II · Eyezone
Key facts
| Recall number (Z-number) | Z-0642-2012 |
|---|---|
| Recall event | 60633 |
| Product | Neulook Fancy FX is packaged in a small glass bottle with a orange, white, and yellow affixed label with black printing that reads, NeuLook COLOR CONTACT LENSES Distributed by EYEZONE Contents : One Lens, 38% water and 62% Polymacon immersed in saline. Caution : To ensure that your contacts stay… |
| Product code | LPL |
| Recalling firm | Eyezone |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 4, 2014 |
| 510(k) numbers | K002099 |
| FEI number | 3009014092 |
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