FDA Enforcement
Class II
Ongoing
Flexiva Pulse ID 242 TracTip single Use Fiber-intended to be used as a device that transmits Ho:YAG laser energy from cleared laser consoles to urological anatomy 5-pack UPN: M006L8406961
Recall: Z-2234-2023
·
Reported August 2, 2023
Enforcement
- Recall Number
- Z-2234-2023
- Event ID
- 92570
- Classification
- Class II
- Status
- Ongoing
- Product Type
- Devices
- Firm
- Boston Scientific Corporation
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- August 2, 2023
- Initiation Date
- May 25, 2023
- Classification Date
- July 21, 2023
- Address
- 100 Boston Scientific Way, N/A, Marlborough, MA, 01752-1234, United States
Description
Flexiva Pulse ID 242 TracTip single Use Fiber-intended to be used as a device that transmits Ho:YAG laser energy from cleared laser consoles to urological anatomy 5-pack UPN: M006L8406961
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 Info
GTIN: 08714729978763 Lot Numbers: 30389516, 30389520, 30389525, 30429871, 30479615 Exp. Date: 20-Oct-2025 to 3-Nov-2025
Distribution
Worldwide distribution - US Nationwide and the country of Canada.
Quantity
280 units