Device recall
Z-2916-2018: Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear, 8.5 Base Curve…
FDA device recall · Class II · Johnson & Johnson Vision Care, Inc.
Key facts
| Recall number (Z-number) | Z-2916-2018 |
|---|---|
| Recall event | 80654 |
| Product | Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear, 8.5 Base Curve, -3.25 Power. Master Lot, containing 12 split lots, repackaged in 30 and 90-packs . Intended for daily disposable wear for the optical correction of refractive ametropia (myopia and hyperopia) in phakic or aphakic persons… |
| Product code | LPL |
| Recalling firm | Johnson & Johnson Vision Care, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 6, 2021 |
| 510(k) numbers | K062614 |
| 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