# FDA recall Z-2425-2019

> **Karl Storz Endoscopy** · Class II · device recall initiated 2019-02-20.

## Product

FLEXIBLE NEURO-FIBERSCOPE, 3.7MM X 34CM, Model # 11282BN1

## Reason for recall

The action is being initiated due to Flexible Neuroscopes manufactured with the incorrect  channel port.

## Distribution

US: FL, MO, MA, AL,CA, OH, PA,NH, OR, WA, MI, NC, CA, VA

## Key facts

- **Recall number:** Z-2425-2019
- **Recalling firm:** Karl Storz Endoscopy
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-02-20
- **Report date:** 2019-09-04
- **Termination date:** 2020-07-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** El Segundo, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2425-2019

## Citation

> AI Analytics. FDA recall Z-2425-2019. Retrieved 2026-05-31 from https://api.ai-analytics.org/recall/Z-2425-2019. Source: US FDA. Licensed CC0.

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