Device recall
Z-2323-2026: TDC VELOCE", 25G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT25…
FDA device recall · Class II · D.O.R.C. Dutch Opthalmic Research Center Intl B.V.
Key facts
| Recall number (Z-number) | Z-2323-2026 |
|---|---|
| Recall event | 98814 |
| Product | TDC VELOCE", 25G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT25, 9311.25G01, 9311.25G02, 9311.25K01, 9311.25K02, 9311.25K03, 9625.G0201; |
| Product code | HQE |
| Recalling firm | D.O.R.C. Dutch Opthalmic Research Center Intl B.V. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K213467 |
| FEI number | 3002806863 |
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