Device recall
Z-0634-03: BD K-3000 Microkeratome Blade REF 378607
FDA device recall · Class II · BD Opthalmic Systems
Key facts
| Recall number (Z-number) | Z-0634-03 |
|---|---|
| Recall event | 25652 |
| Product | BD K-3000 Microkeratome Blade REF 378607 |
| Product code | HMY |
| Recalling firm | BD Opthalmic Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 28, 2003 |
| 510(k) numbers | K022637 |
| FEI number | 1211998 |
At a glance
- 1–9 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