Checkpoint Surgical recalls medium-sized intraoperative leads due to potential electrical leakage causing inconsistent muscle responses during surgery. Affected units have specific model numbers and expiration dates.
Adhesive on the back of the lead may not fully encapsulate the metallic portion of the wire and button subassembly, potentially leading to exposed metal. There is a risk of electrical current leakage, which may lead to inconsistent or confusing muscle responses, potentially compromising the effectiveness of the intended use as the surgeon could take an incorrect clinical action.
Checkpoint Surgical recalls medium-sized intraoperative leads that may cause electrical leakage, leading to inconsistent muscle responses and potential surgical errors. This could affect surgeons using the leads during procedures.
The adhesive on the lead's back may not fully cover the metal parts, causing electrical current leakage. This could lead to inconsistent muscle responses, potentially causing surgeons to make incorrect decisions during surgery.
Surgeons using Checkpoint Guardian Intraoperative Leads, Medium size, for nerve stimulation during surgery. Those with the specific model numbers (REF# 9525) and expiration dates listed are most at risk.
Check for the model number REF# 9525 (Medium) on the product. The leads expire by specific dates: April 1, 2026, July 1, 2026, and other dates listed in the recall notice.
Look for the model number REF# 9525 (Medium) and expiration dates listed in the recall notice.
The specific model number is REF# 9525 (Medium).
The risk is electrical leakage that could cause inconsistent muscle responses, potentially leading to surgical errors.
The leads expire by specific dates: April 1, 2026, July 1, 2026, and other dates listed in the recall notice.
We’ve drafted a message you can send Checkpoint to request your refund or repair — edit it as you like.
Subject: Recall Z-1467-2025 — Checkpoint Checkpoint Hello, I own a Checkpoint that is covered by recall Z-1467-2025 from Checkpoint. 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.
