Device recall
Z-1865-2021: ACUVUE VITA soft (hydrophilic) contact lens (spherical) for daily wear. Base…
FDA device recall · Class II · Johnson & Johnson Vision Care, Inc.
Key facts
| Recall number (Z-number) | Z-1865-2021 |
|---|---|
| Recall event | 87947 |
| Product | ACUVUE VITA soft (hydrophilic) contact lens (spherical) for daily wear. Base Curve 8.8, Refractive Power -1.50 |
| Product code | LPL |
| Recalling firm | Johnson & Johnson Vision Care, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 2, 2021 |
| 510(k) numbers | K160212 |
| FEI number | 1000222023 |
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