Active Cord M00561250Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 08714729019060), received between Jul 14, 2021 and Jul 14, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device-Device Incompatibility” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 14, 2021Device-Device Incompatibility; Appropriate Device Problem Term/Code Not Available; Device-Device Incompatibility; Appropriate Device Problem Term/Code Not Available

  IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT AN ACTIVE CORD OLYMPUS DEVICE WAS TO BE USED DURING A POLYPECTOMY PROCEDURE PERFORMED ON (B)(6) 2021. IT WAS REPORTED THAT OUTSIDE THE PATIENT, AN ELECTROCAUTERY SCALPEL MADE BY SENKO MEDICAL AND A CONNECTOR ON THE MAIN SIDE WAS CONNECTED WITHOUT ANY PROBLEM. HOWEVER, WHEN CONNECTED TO A CAPTIVE, THE CONNECTOR ON THE SNARE SIDE WAS LOOSE AND UNSTABLE. THEY TRIED CONNECTING TO A NON-BSC SNARE BUT IT WAS LOOSE AND UNSTABLE AS WELL. NO OTHER ISSUES WERE NOTED WITH THE DEVICE. THE PROCEDURE WAS DISCONTINUED AND THE TARGET TREATMENT WAS NOT COMPLETED. HOWEVER, THE PHYSICIAN WAS PLANNING ON COMPLETING THE PROCEDURE AND HAS ALREADY ORDERED A NON-BSC ACTIVE CORD. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12165674 ↗