Official recall notice

FDA DeviceClass IINotable

HOPKINS Telescope 30 Recall (Oct 2026) – Karl Storz Endoscopy

Product: 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.

Recall date
2026-10-07
FDA class
Class II

Why it was recalled

Hazard

Due to incorrect inside packaging label for eyepiece.

One email a week when there are new recalls. Confirm by email; unsubscribe anytime.

Product description

Due to incorrect inside packaging label for eyepiece.

Affected products

Material Number: 10005BA UDI-DI code: 04048551045121 Serial Numbers: 100011, 100012, 10000Y, and 10000Z

Verify with the official notice →
Share:

Related Recalls

2026-10-07 · FDA_DEVICE
FDA Recall: Ingenia Ambition S and Ingenia Ambition X.; Model number (REF): 1. 781359 (S), 2. 782108 (S), 3. 78
Philips North America
2026-10-07 · FDA_DEVICE
FDA Recall: CHARLOTTE CLAW Screw, REF: 40122716, intended for use with CLAW II Polyaxial Compression Plating Sys
Wright Medical Technology, Inc.
2026-10-07 · FDA_DEVICE
FDA Recall: Ingenia Blue Seal SE and Blue Seal XE; Model number (REF): 1. 782185 (SE), 2. 782192 (XE); Softwar
Philips North America
2026-10-07 · FDA_DEVICE
FDA Recall: Travel Air, Product Number: S00055; Phasitron 5, Product Number: P5 used with Instruction Manual
Percussionaire Corporation