# FDA recall Z-2776-2026

> **Olympus Corporation of the Americas** · Class II · device recall initiated 2026-06-16.

## Product

Olympus High Flow Insufflation Unit - UHI-4. Model Number: UHI-4

## Reason for recall

Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases.

## Distribution

Worldwide distribution - US Nationwide and the countries of Australia, Bolivia, Brazil, Canada, Chile, China, Colombia, Costa Rica, Ecuador, El Salvador, Germany, Honduras, Hong Kong, India, Ireland, Japan, Korea, Malaysia, Mexico, Myanmar, New Zealand, Paraguay, Peru, Russia, Singapore, Sri Lanka, Taiwan, Thailand, United Kingdom, Uruguay, Vietnam.

## Key facts

- **Recall number:** Z-2776-2026
- **Recalling firm:** Olympus Corporation of the Americas
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-06-16
- **Report date:** 2026-07-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Center Valley, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2776-2026

## Citation

> AI Analytics. FDA recall Z-2776-2026. Retrieved 2026-09-01 from https://api.ai-analytics.org/recall/Z-2776-2026. Source: US FDA. Licensed CC0.

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