Device recall
Z-1821-2020: Alcon Air Optix Night & Day Aqua (lotrafilcon A), breathable contact lenses, PWR…
FDA device recall · Class II · Allied Vision Group Inc
Key facts
| Recall number (Z-number) | Z-1821-2020 |
|---|---|
| Recall event | 84839 |
| Product | Alcon Air Optix Night & Day Aqua (lotrafilcon A), breathable contact lenses, PWR - 1.50 BC 8.6 DIA 13.8, Rx, Sterile. The firm name on the label is Alcon Laboratories, Inc., Fort Worth, TX. |
| Product code | LPM |
| Recalling firm | Allied Vision Group Inc |
| Recall class | Class II |
| Status | Completed |
| PMA numbers | P010019 |
| FEI number | 1000122287 |
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