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Recall Observatory FDA recall evidence

Device product

Flexiva Pulse ID-intended to be used as a device that transmits Ho:YAG laser energy from cleared laser consoles to urological anatomy (Box of 5)UPN: M006L8406911

Z-2232-2023

May 25, 2023

Class II

Product summary

Firm
Boston Scientific Corporation
Event
Event 92570
Status
Ongoing
Classification
Class II
Quantity
205 units
Official record key
device-enforcement:Z-2232-2023

Official wording

Reason: 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

Code information: GTIN: 08714729978725 Lot Numbers: 30521480, 30521485 ,30521486 Exp. Date: 20-OCT-2024 to 10-Nov-2025

Distribution pattern: Worldwide distribution - US Nationwide and the country of Canada.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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