Device recall
Z-0445-2012: Crystalens Accommodating Posterior Chamber Intraocular Lens, AT-50AO. Crystalens…
FDA device recall · Class II · Bausch and Lomb, Incorporated
Key facts
| Recall number (Z-number) | Z-0445-2012 |
|---|---|
| Recall event | 60565 |
| Product | Crystalens Accommodating Posterior Chamber Intraocular Lens, AT-50AO. Crystalens Accommodating Posterior Chamber Intraocular Lens PMA No.: P030002. The Crystalens is intended for primary implantation in the capsular bag of the eye for the visual correction of aphakia secondary to the removal of a… |
| Product code | NAA |
| Recalling firm | Bausch and Lomb, Incorporated |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 23, 2012 |
| PMA numbers | P030002 |
| FEI number | 3004343135 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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