Boston Scientific recalls GreenLight HPSEA Laser Fibers (UPN 0010-2092) due to fiber type mismatch errors causing procedure delays. Affected units may need replacement to avoid extended surgery times.
Several complaints were received for the affected lot; users received a "Fiber type does not match card type" error message on the GreenLight XPS Laser console, necessitating the replacement of the laser fiber and fiber card. This may result in prolonged procedure while the fiber is being replaced.
Boston Scientific is recalling GreenLight HPSEA Laser Fibers with a specific UPC code because they sometimes show a 'fiber type does not match card type' error. This error can cause surgery to take longer while technicians replace the fiber and card.
The fiber and card combination sometimes causes an error message that requires replacing both components. This interruption can delay surgery procedures until the mismatched parts are fixed.
Surgical staff using the GreenLight XPS Laser system with the recalled fiber model are most affected. Patients undergoing procedures with this specific fiber may experience longer surgery times.
Check for the UPC code 00878953005522 on the fiber packaging or label. The affected lot number is 27770466. This recall applies to GreenLight HPSEA Laser Fibers sold with the UPN 0010-2092.
Look for a 'Fiber type does not match card type' error on the GreenLight XPS Laser console during surgery.
Reach out to Boston Scientific for assistance with replacing the fiber and card if the error occurs.
The recall is due to a fiber type mismatch error that requires replacing the laser fiber and card, which can delay surgery procedures.
Check the UPC code 00878953005522 on the fiber packaging or label. The affected lot number is 27770466.
Contact Boston Scientific to replace the fiber and card to avoid extended surgery times.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-1392-2022 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-1392-2022 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.
