Olympus Corporation Of The Americas Olympus ShockPulse-SE Lithotripsy System with Generator: ShockPulse-SE Lithotripsy System

Source: FDA | Recall date: 03/11/2026

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Affected product: Olympus ShockPulse-SE Lithotripsy System with Generator: ShockPulse-SE Lithotripsy System - Reuseable Probes Model/Catalog Number: SPL-SR, contains generator SPL-G Product Description: An assembly of devices that uses a

Brand: olympus corporation of the americas

Hazard: Mis-wired component-the improperly wired component can result in additional noise on the power supply output. Noise on the ultrasonic input circuit is not consistent with electromagnetic compatibility (EMC) standards and may decrease the overall reliability of the system and resu

Official identifiers

FDA recall number: Z-1494-2026
FDA event number: 98360

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