FDA Device recall Z-2776-2026
Olympus High Flow Insufflation Unit - UHI-4. Model Number: UHI-4
- FDA Device
- Class II
- ongoing
- Published 2026-07-29
On 2026-07-29 the FDA classified a Class II recall of Olympus High Flow Insufflation Unit - UHI-4. Model Number: UHI-4 by Olympus, citing potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2776-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-06-16 |
| Published | 2026-07-29 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Olympus |
| Distribution | US |
Product
Olympus High Flow Insufflation Unit - UHI-4. Model Number: UHI-4
Reason
Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases.
Identifiers
| code_info | Model Number: UHI-4. UDI: 04953170324147, 04953170467219. All Serial Numbers. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
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FDA Device · Class II · 2026-10-07 · Olympus - Olympus BiCOAG Hemostasis Probe 7Fr Coaxial Connector
FDA Device · Class II · 2026-09-30 · Olympus - Olympus EZDilate Endoscopic Balloon Dilator Wired-guided 11, 12, 13mm
FDA Device · Class II · 2026-09-30 · Olympus
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2776-2026%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.