# FDA recall Z-2292-2020

> **Olympus Corporation of the Americas** · Class II · device recall initiated 2020-05-05.

## Product

ENF-GP2 Rhino-Laryngo Fiberscope - Product Usage: is indicated for use within the nasal and nasopharyngeal lumen.

## Reason for recall

Products repaired with the incorrect service manual may be missing an O ring and are subject to rework with the corrected service manual.

## Distribution

US Nationwide distribution including in the states of FL, MI, NM, NY, OH, and OR. No international distribution.

## Key facts

- **Recall number:** Z-2292-2020
- **Recalling firm:** Olympus Corporation of the Americas
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-05-05
- **Report date:** 2020-06-17
- **Termination date:** 2020-09-18

- **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-2292-2020

## Citation

> AI Analytics. FDA recall Z-2292-2020. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/Z-2292-2020. Source: US FDA. Licensed CC0.

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