# FDA recall Z-1052-2025

> **Karl Storz Endoscopy** · Class II · device recall initiated 2024-12-19.

## Product

KARL STORZ - ENDOSKOPE, REF: 27030KA, Cysto-Urethroscope, NON STERILE, CE

## Reason for recall

Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1052-2025
- **Recalling firm:** Karl Storz Endoscopy
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-12-19
- **Report date:** 2025-02-05

- **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-1052-2025

## Citation

> AI Analytics. FDA recall Z-1052-2025. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1052-2025. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*