Device recall
Z-2153-2011: Circumcision Clamp, models 1.1 cm and 1.3 cm, Circumcision clamp is an…
FDA device recall · Class II · Surgical Design Inc
Key facts
| Recall number (Z-number) | Z-2153-2011 |
|---|---|
| Recall event | 58318 |
| Product | Circumcision Clamp, models 1.1 cm and 1.3 cm, Circumcision clamp is an instrument used to compress the foreskin of the penis during circumcision of a male infant. |
| Product code | HFX |
| Recalling firm | Surgical Design Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 21, 2013 |
| 510(k) numbers | K043533 |
| FEI number | 3001236105 |
At a glance
- 1–9 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