Device recall
Z-0989-2018: Alden Classic 55 Toric Daily Wear Soft contact; Catalog Number: AOCLT55 Product…
FDA device recall · Class II · Alden Optical
Key facts
| Recall number (Z-number) | Z-0989-2018 |
|---|---|
| Recall event | 79377 |
| Product | Alden Classic 55 Toric Daily Wear Soft contact; Catalog Number: AOCLT55 Product Usage: The ALDEN TORIC LENS for daily wear is indicated for the correction of visual acuity in aphakic and not aphakic persons with non-diseased eyes with refractive ametropia (myopia or hyperopia) and/or possesses… |
| Product code | LPL |
| Recalling firm | Alden Optical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 19, 2018 |
| 510(k) numbers | K042242 |
| FEI number | 1315522 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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