Device recall
Z-0066-2008: BD Microkeratome K3000 and K4000;Catalog Number: 378660, Becton Dickinson &…
FDA device recall · Class II · Becton Dickinson and Company
Key facts
| Recall number (Z-number) | Z-0066-2008 |
|---|---|
| Recall event | 38739 |
| Product | BD Microkeratome K3000 and K4000;Catalog Number: 378660, Becton Dickinson & Company (BD) |
| Product code | HMY |
| Recalling firm | Becton Dickinson and Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 29, 2012 |
| 510(k) numbers | K023092 |
| 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