KARL STORZ - ENDOSKOPE, REF: 27000L,Uretero-Renoscope, 7 Fr., 6¿, 43 cm, NON STERILE, RxONLY, CE...

FDA Recall #Z-1056-2025 — Class II — December 19, 2024

Recall #Z-1056-2025 Date: December 19, 2024 Classification: Class II Status: Ongoing

Product Description

KARL STORZ - ENDOSKOPE, REF: 27000L,Uretero-Renoscope, 7 Fr., 6¿, 43 cm, NON STERILE, RxONLY, CE 0123

Reason for Recall

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

Recalling Firm

Karl Storz Endoscopy — El Segundo, CA

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

65 units

Distribution

US Nationwide distribution.

Code Information

All Lots/UDI: 04048551311271

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated