HOPKINS Telescope 30¿, 4mm REF 10005BA UDI-DI code: 04048551045121 KARL STORZ HOPKINS¿ and HOPKINS¿ II telescopes are to be used for visualization of the surgical site during diagnostic and therapeutic endoscopic procedures.

Class II

Recalling firm: Karl Storz Endoscopy
Reason for recall: Due to incorrect inside packaging label for eyepiece.
Affected products (lot / model / serial): Material Number: 10005BA UDI-DI code: 04048551045121 Serial Numbers: 100011, 100012, 10000Y, and 10000Z
Units affected: 6 eyepieces
Distribution pattern: U.S. Nationwide distribution in the states of AZ, CA and MO.
Firm location: El Segundo, CA, United States
Recall type: Voluntary: Firm initiated
How the firm notified customers: Letter
Product type: Devices
Status: Ongoing
Recall number: Z-3333-2026
Recall initiated: August 12, 2026
FDA classification date: September 30, 2026
FDA report date: October 7, 2026
FDA event ID: 99586
Last updated on HTM Vibe: October 13, 2026