Device recall
Z-2151-2021: MEDIFLEX ELITE 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens…
FDA device recall · Class II · CooperVision Inc.
Key facts
| Recall number (Z-number) | Z-2151-2021 |
|---|---|
| Recall event | 88096 |
| Product | MEDIFLEX ELITE 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker |
| Product code | LPL |
| Recalling firm | CooperVision Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 13, 2023 |
| 510(k) numbers | K130331 |
| FEI number | 3005724763 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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