N/A LF1212ARecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613327565300), received between Oct 17, 2025 and Oct 17, 2025 — classified as 3 injuries.

The most frequently reported specific device problem is “Contamination” (3 reports).

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryOct 17, 2025Contamination; Device Appears to Trigger Rejection; Contamination; Device Appears to Trigger Rejection

  IT WAS REPORTED THAT THE REPROCESSED LIGASURE FAILED. IT WAS NOTICED BY THE PHYSICIAN THAT THE HYSTERECTOMY INFECTION THAT HE ASSISTED WITH HAD USED A REPROCESSED LIGASURE DEVICE DURING THE CASE. THE COMPLAINANT IS NOT AWARE OF ANY PATIENT INJURY, MEDICAL INTERVENTION, OR EXTENDED PROCEDURE TIME. THESE ARE COMMONLY USED DEVICES THAT ARE READILY AVAILABLE.

  Patient problems: Insufficient Information; Unspecified Infection

  MAUDE report 23330399 ↗
• InjuryOct 17, 2025Contamination; Device Appears to Trigger Rejection; Contamination; Device Appears to Trigger Rejection

  IT WAS REPORTED THAT THE REPROCESSED LIGASURE FAILED. IT WAS NOTICED BY THE PHYSICIAN THAT THE HYSTERECTOMY INFECTION THAT HE ASSISTED WITH HAD USED A REPROCESSED LIGASURE DEVICE DURING THE CASE. THE COMPLAINANT IS NOT AWARE OF ANY PATIENT INJURY, MEDICAL INTERVENTION, OR EXTENDED PROCEDURE TIME. THESE ARE COMMONLY USED DEVICES THAT ARE READILY AVAILABLE.

  Patient problems: Insufficient Information; Unspecified Infection

  MAUDE report 23330397 ↗
• InjuryOct 17, 2025Contamination; Device Appears to Trigger Rejection; Contamination; Device Appears to Trigger Rejection

  IT WAS REPORTED THAT THE REPROCESSED LIGASURE FAILED. IT WAS NOTICED BY THE PHYSICIAN THAT THE HYSTERECTOMY INFECTION THAT HE ASSISTED WITH HAD USED A REPROCESSED LIGASURE DEVICE DURING THE CASE. THE COMPLAINANT IS NOT AWARE OF ANY PATIENT INJURY, MEDICAL INTERVENTION, OR EXTENDED PROCEDURE TIME. THESE ARE COMMONLY USED DEVICES THAT ARE READILY AVAILABLE.

  Patient problems: Insufficient Information; Unspecified Infection

  MAUDE report 23330395 ↗