Olympus High Flow Insufflation Unit - UHI-4
Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases.
- Agency
- FDA Device
- Recall date
- Jun 16, 2026
- Status
- Ongoing
- Company
- Olympus Corporation of the Americas
1. What product was recalled?
Olympus High Flow Insufflation Unit - UHI-4
Olympus High Flow Insufflation Unit - UHI-4. Model Number: UHI-4
Quantity: 3,087 units
Code or lot text: Model Number: UHI-4. UDI: 04953170324147, 04953170467219. All Serial Numbers.
- LOT
- 04953170467219. All Serial Numbers.
- LOT
- Model Number: UHI-4. UDI: 04953170324147
- RECALL-NUMBER
- Z-2776-2026
2. Is my exact product affected?
Compare every printed identifier. A matching value can indicate that your product is included.
3. What is the hazard?
Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases.
4. What should I do now?
Follow the FDA recall notice and contact the recalling company for current instructions.
5. Where was it sold or distributed?
Nationwide
6. Were injuries or illnesses reported?
No separate injury or illness statement was present in the normalized record. Check the official source for the latest report.
7. What remedy is available?
Follow the FDA recall notice and contact the recalling company for current instructions.
8. Is the recall active or closed?
The source status is Ongoing. Recall Index urgency is elevated, which is a separate deterministic site label.
9. When was the information checked?
Last checked .
- created
10. Where is the official source?
Open the official FDA Device source
Recall Index normalizes public source data for easier checking. Source agencies remain authoritative. Confirm identifiers and instructions at the official source.