# FDA recall Z-1274-2022

> **Olympus Corporation of the Americas** · Class II · device recall initiated 2022-04-22.

## Product

Colonovideoscope   Model CF-H180AL

## Reason for recall

A (Camera unit) CCD intended for a different model of colonoscope may have been installed in the CF-H180AL, viewing angle would be narrower than a normal CF-H180AL and the use of EndoTherapy devices may stick out (approximately 1.4 mm) further than normal protrusion,could lead to patient injury; specifically, mucosal damage that could result in hemorrhage or bleeding

## Distribution

US Nationwide distribution in the state of KY.

## Key facts

- **Recall number:** Z-1274-2022
- **Recalling firm:** Olympus Corporation of the Americas
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-04-22
- **Report date:** 2022-06-29
- **Termination date:** 2024-03-13

- **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-1274-2022

## Citation

> AI Analytics. FDA recall Z-1274-2022. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1274-2022. Source: US FDA. Licensed CC0.

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