Device recall
Z-2364-2023: UroLift Visual Obturator, 20Ch-The visual obturator is used with the UroLift…
FDA device recall · Class II · Scholly Fiberoptic Gmbh
Key facts
| Recall number (Z-number) | Z-2364-2023 |
|---|---|
| Recall event | 92700 |
| Product | UroLift Visual Obturator, 20Ch-The visual obturator is used with the UroLift system. Instrument for insertion of a cystoscope shaft into the bladder. Model: UL-VO |
| Product code | HIH |
| Recalling firm | Scholly Fiberoptic Gmbh |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K150158 |
| FEI number | 3002808088 |
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