Device recall
Z-0274-2009: PurePoint System Operator's Manual, Catalog Number 8065751131, Rev. B for use…
FDA device recall · Class II · Alcon Laboratories, Inc.
Key facts
| Recall number (Z-number) | Z-0274-2009 |
|---|---|
| Recall event | 49600 |
| Product | PurePoint System Operator's Manual, Catalog Number 8065751131, Rev. B for use with the Alcon PurePoint Laser, Catalog Number 8065750597 Indicated for use in photocoagulation of both anterior and posterior segments of the eye. |
| Product code | HQF |
| Recalling firm | Alcon Laboratories, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 7, 2012 |
| FEI number | 1000125771 |
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