Device recall
Z-1455-2025: Brand Names: MyDay Toric, LensCrafters One Day Premium Daily Disposable Contact…
FDA device recall · Class II · CooperVision, Inc.
Key facts
| Recall number (Z-number) | Z-1455-2025 |
|---|---|
| Recall event | 96396 |
| Product | Brand Names: MyDay Toric, LensCrafters One Day Premium Daily Disposable Contact Lenses For Astigmatism, Pearle Vision 1 Day Premium For Astigmatism, REVEAL 1-DAY TORIC, Vision Source Reveal Toric, Voyant 1-Day Premium Toric. Brand Names (OUS only): CADENCE DELUXE 1-DAY TORIC, DUBLAN PREMIUM OXYGEN 1… |
| Product code | MVN |
| Recalling firm | CooperVision, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K131378, K190965, K220070 |
| FEI number | 3005724763 |
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