# FDA recall Z-2480-2023

> **Olympus Corporation of the Americas** · Class II · device recall initiated 2023-07-20.

## Product

Visera Hysterovideoscope Olympus HYF Type V

## Reason for recall

IFU labeling is being updated to revise EtO gas mixture and elimination of reusable cleaning brushes.

## Distribution

US Nationwide distribution including in the states of AL, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NE, NJ, NM, NV, NY, OH, OR, PA, RI, SC, SD, TX, UT, WA, and WI.

## Key facts

- **Recall number:** Z-2480-2023
- **Recalling firm:** Olympus Corporation of the Americas
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-07-20
- **Report date:** 2023-09-06

- **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-2480-2023

## Citation

> AI Analytics. FDA recall Z-2480-2023. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2480-2023. Source: US FDA. Licensed CC0.

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