Karl Storz Endoscopy: Medical Device Recall in 2025 - (Recall #: Z-1056-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: December 19, 2024

Date Posted: February 5, 2025

Recall Number: Z-1056-2025

Event ID: 95975

Reason for Recall:

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

Status: Ongoing

Product Quantity: 65 units

Code Information:

All Lots/UDI: 04048551311271

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated