Device recall
Z-0708-03: DeRoyal''s SurgiMate (tm) Skin Stapler, Rotating Head, product #25-1001…
FDA device recall · Class II · Deroyal Surgical -Rose Hill
Key facts
| Recall number (Z-number) | Z-0708-03 |
|---|---|
| Recall event | 25788 |
| Product | DeRoyal''s SurgiMate (tm) Skin Stapler, Rotating Head, product #25-1001, packaged with 35 or more stainless steel staples in peel away pouch. Pouch is labeled in part, ***sterile, disposable, do not resterilize***. Pouches are packaged 12 per box. |
| Product code | MNV |
| Recalling firm | Deroyal Surgical -Rose Hill |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 7, 2003 |
| FEI number | 1046367 |
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