Device recall
Z-0705-03: Sharpoint ClearTrap Trapezoid Clear Corneal/Implant Knife. Ophthalmic Knife 2.5…
FDA device recall · Class II · Surgical Specialties Corp
Key facts
| Recall number (Z-number) | Z-0705-03 |
|---|---|
| Recall event | 25816 |
| Product | Sharpoint ClearTrap Trapezoid Clear Corneal/Implant Knife. Ophthalmic Knife 2.5 mm x 3.5 mm. |
| Product code | HNN |
| Recalling firm | Surgical Specialties Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 31, 2003 |
| 510(k) numbers | K822112 |
| FEI number | 2522801 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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