# FDA recall Z-0557-2024

> **Olympus Corporation of the Americas** · Class II · device recall initiated 2023-09-28.

## Product

TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP, Model Number: LF-GP

## Reason for recall

Fiberscopes do not have adequate data to support that the suction flow rate meets the device specification.

## Distribution

Worldwide - US Nationwide distribution in the states of AK, AL, AZ, CA, GA, IL, IN, MA, MD, MI, NC, NJ, OH, TX, UT, VA, WA, WV & AP (Armed Forces Pacific) and the countries of OUS: EMEA, Japan and Australia.

## Key facts

- **Recall number:** Z-0557-2024
- **Recalling firm:** Olympus Corporation of the Americas
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-09-28
- **Report date:** 2023-12-20

- **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-0557-2024

## Citation

> AI Analytics. FDA recall Z-0557-2024. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-0557-2024. Source: US FDA. Licensed CC0.

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