Device recall
Z-0629-2007: EpiFix Fixation Device for Epidural Catheters, REF 670M, Unomedical, Ltd., Great…
FDA device recall · Class II · Merit Medical Systems, Inc
Key facts
| Recall number (Z-number) | Z-0629-2007 |
|---|---|
| Recall event | 37422 |
| Product | EpiFix Fixation Device for Epidural Catheters, REF 670M, Unomedical, Ltd., Great Britain. |
| Product code | KMK |
| Recalling firm | Merit Medical Systems, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 9, 2011 |
| FEI number | 1721504 |
At a glance
- None 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