Device recall
Z-0561-2007: Alcon Custom-Pak, part #2638-17, containing BD Beaver Mini-Blade (part #BD6400…
FDA device recall · Class II · Alcon Laboratories, Inc
Key facts
| Recall number (Z-number) | Z-0561-2007 |
|---|---|
| Recall event | 37153 |
| Product | Alcon Custom-Pak, part #2638-17, containing BD Beaver Mini-Blade (part #BD6400 or part #BD6900); individual blades repackaged into custom ophthalmic surgical packs and resterilized by Alcon Laboratories, Inc., Houston, TX. |
| Product code | HNN |
| Recalling firm | Alcon Laboratories, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 6, 2007 |
| FEI number | 1000117501 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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