medical Class II Updated 2023-08-02

Boston Scientific Corporation recalls Flexiva Pulse 242 ID Trac Single Use Fiber-intended to be us

Recalled Product

Flexiva Pulse 242 ID Trac Single Use Fiber-intended to be used as a device that transmits Ho:YAG laser energy from cleared laser consoles to urological anatomy (Single-pack UPN): M006L8406960


Hazard / Issue

Manufactured with the incorrect component may result in lower power output and degradation or dimming of the aiming beam, leading to reduced efficiency of fiber performance. Continued use may cause overheating of the fiber connector, which could result in a burn, if touched

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: GTIN: 08714729978718 Lot Numbers: 30261914, 30389513, 30429863, 30429864, 30479612 Exp. Date: 02-Oct-2025 to 3-Nov-2025
View official government recall

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