Device recall
Z-2109-2013: ACCU-CHECK FastClix Lancing Device. It is intended for use in conjunction with a…
FDA device recall · Class II · Roche Diagnostics Operations, Inc.
Key facts
| Recall number (Z-number) | Z-2109-2013 |
|---|---|
| Recall event | 65886 |
| Product | ACCU-CHECK FastClix Lancing Device. It is intended for use in conjunction with a blood glucose monitoring system. |
| Product code | FMK |
| Recalling firm | Roche Diagnostics Operations, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 12, 2014 |
| FEI number | 1823260 |
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