# FDA recall Z-1208-2024

> **Olympus Corporation of the Americas** · Class II · device recall initiated 2024-01-11.

## Product

Colonoscope, Model Number CF-Q180AL.

## Reason for recall

Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration, fluctuation in temperature or severe shock loads.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1208-2024
- **Recalling firm:** Olympus Corporation of the Americas
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-01-11
- **Report date:** 2024-03-06

- **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-1208-2024

## Citation

> AI Analytics. FDA recall Z-1208-2024. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1208-2024. Source: US FDA. Licensed CC0.

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