Device recall
Z-0348-03: OPTIMA FW (polymacon) Visibility Tinted Contact Lenses, labeled as -2.25D, 8.7…
FDA device recall · Class III · Bausch & Lomb Inc
Key facts
| Recall number (Z-number) | Z-0348-03 |
|---|---|
| Recall event | 25105 |
| Product | OPTIMA FW (polymacon) Visibility Tinted Contact Lenses, labeled as -2.25D, 8.7 mm. Responsible firm on the label: Bausch & Lomb Inc., Rochester, NY 14692. Each box contains six lenses. |
| Product code | LPM |
| Recalling firm | Bausch & Lomb Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 23, 2003 |
| FEI number | 1317628 |
At a glance
- None 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