Boston Scientific recalls Flexiva Pulse 242 ID Trac Single Use Fiber due to potential laser beam dimming and overheating risks. Affected units have specific lot numbers and expiration dates.
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
Boston Scientific is recalling Flexiva Pulse 242 ID Trac Single Use Fiber devices that may dim the laser beam and cause overheating, potentially leading to burns if touched. This recall affects specific lot numbers and expiration dates.
The device may have incorrect components causing the laser beam to dim and reduce efficiency. Continued use could lead to overheating at the fiber connector, potentially causing burns if touched.
Urology professionals using the Flexiva Pulse 242 ID Trac Single Use Fiber for laser procedures are most at risk. The recall applies to specific lot numbers and expiration dates.
Check for lot numbers 30261914, 30389513, 30429863, 30429864, or 30479612 with expiration dates between February 2025 and November 2025.
Look for lot numbers 30261914, 30389513, 30429863, 30429864, or 30479612 on the device packaging.
If the laser beam appears dimmed or the device overheats, stop using it immediately and contact Boston Scientific.
Boston Scientific recalls Flexiva Pulse 242 ID Trac Single Use Fiber devices that may dim the laser beam and cause overheating, potentially leading to burns if touched.
Units with lot numbers 30261914, 30389513, 30429863, 30429864, or 30479612 and expiration dates between February 2025 and November 2025.
Check the lot number and expiration date. If the device is dimmed or overheating, stop using it and contact Boston Scientific.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-2233-2023 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-2233-2023 from Boston Scientific. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
