Device recall
Z-0135-2026: C-Rex UNO Microinterventional Goniotomy Instrument. Model Number: CRX-120…
FDA device recall · Class II · Iantrek Inc.
Key facts
| Recall number (Z-number) | Z-0135-2026 |
|---|---|
| Recall event | 97640 |
| Product | C-Rex UNO Microinterventional Goniotomy Instrument. Model Number: CRX-120. Product Description: The C-Rex UNO Microinterventional Goniotomy Instrument is a sterile single use disposable manual surgical instrument used in ophthalmic procedures for ab interno goniotomy and inner wall trabeculotomy. |
| Product code | HMZ |
| Recalling firm | Iantrek Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3017891009 |
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