Device recall
Z-0710-2007: Sea-Clens Wound Cleanser, 6 fl. oz., Manufactured by Coloplast Corp., Marietta…
FDA device recall · Class II · Coloplast Corp Skin Care Div
Key facts
| Recall number (Z-number) | Z-0710-2007 |
|---|---|
| Recall event | 37597 |
| Product | Sea-Clens Wound Cleanser, 6 fl. oz., Manufactured by Coloplast Corp., Marietta, GA, #11701-159-36, #1063. |
| Product code | KMF |
| Recalling firm | Coloplast Corp Skin Care Div |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 25, 2007 |
| 510(k) numbers | K983519 |
| FEI number | 2125337 |
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