n.a. 11275ZERecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 04048551050576), received between Aug 14, 2025 and Feb 3, 2026 — classified as 2 injuries, 1 malfunction.

The most frequently reported specific device problem is “Mechanical Jam” (2 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. 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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 3, 2026Break

  IT WAS REPORTED THAT "GRASPING MECHANISM OF THE INSTRUMENT BROKE WHILST IN USE ON A PATIENT. THE SURGEON NEEDED TO CLOSE THE JAWS TO SAFELY REMOVE THEM FROM THE PATIENT, BUT STRUGGLED TO DO SO. THEY MANAGED TO CLOSE THE JAW, REMOVE THE INSTRUMENT, AND PROCEED WITH THE CASE USING A SECOND INSTRUMENT." THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED.

  Patient problems: Insufficient Information

  MAUDE report 24245973 ↗
• InjuryAug 14, 2025Use of Device Problem; Mechanical Jam; Mechanical Jam

  IT WAS REPORTED THAT THE FORCEPS NO LONGER CAN BE OPENED DURING PROCEDURE. THE PROCEDURE WAS NOT SUCCESSFULLY FINISHED SINCE THE SURGEON WAS NOT ABLE TO REMOVE ALL THE SAMPLES. NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22806542 ↗
• InjuryAug 14, 2025Mechanical Jam; Mechanical Jam

  IT WAS REPORTED THAT THE FORCEPS NO LONGER CAN BE OPENED DURING PROCEDURE. THE PROCEDURE WAS NOT SUCCESSFULLY FINISHED SINCE THE SURGEON WAS NOT ABLE TO REMOVE ALL THE SAMPLES. NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22806527 ↗