FDA Device recall Z-2480-2023
Visera Hysterovideoscope Olympus HYF Type V
- FDA Device
- Class II
- ongoing
- Published 2023-09-06
On 2023-09-06 the FDA classified a Class II recall of Visera Hysterovideoscope Olympus HYF Type V by Olympus, citing IFU labeling is being updated to revise EtO gas mixture and elimination of reusable cleaning brushes.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2480-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-07-20 |
| Published | 2023-09-06 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Olympus |
| Distribution | US |
Product
Visera Hysterovideoscope Olympus HYF Type V
Reason
IFU labeling is being updated to revise EtO gas mixture and elimination of reusable cleaning brushes.
Identifiers
| code_info | Model HYF-V, all serial numbers |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2480-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.