Device recall
Z-0734-2012: Outer Carton labeled in part:" 1-DAY ACUVUE MOIST BRAND CONTACT LENSES WITH…
FDA device recall · Class III · Johnson & Johnson Vision Care, Inc.
Key facts
| Recall number (Z-number) | Z-0734-2012 |
|---|---|
| Recall event | 60810 |
| Product | Outer Carton labeled in part:" 1-DAY ACUVUE MOIST BRAND CONTACT LENSES WITH LACREON FOR ASTIGMATISM***Contact Lenses for Daily Wear***D -1.50***-1.25 100***2016/07***BC 8.5***DIA 14.5***Made in USA***LOT B00BVTN0VS***" Individual Lenses labeled in part: "***1-DAY ACUVUE MOIST FOR ASTIGMATISM WITH… |
| Product code | MVN |
| Recalling firm | Johnson & Johnson Vision Care, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 18, 2012 |
| 510(k) numbers | K051900 |
| 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