Device recall
Z-1647-2008: Seprafilm Adhesion Barrier (chemically modified sodium…
FDA device recall · Class II · Genzyme Corporation
Key facts
| Recall number (Z-number) | Z-1647-2008 |
|---|---|
| Recall event | 47758 |
| Product | Seprafilm Adhesion Barrier (chemically modified sodium hyaluronate/carboxymethylcellulose absorbable adhesion barrier) Product Number: 4301-02 |
| Recalling firm | Genzyme Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 29, 2015 |
| PMA numbers | P950034 |
| FEI number | 1220423 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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