V. Mueller SU2804Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10885403064609), received between Apr 20, 2022 and Jun 19, 2025 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Break” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 19, 2025Break; Break

  THE USER FACILITY REPORTED THAT A TIP FROM THEIR OCHSNER ARTERY FORCEPS BROKE OFF DURING A PATIENT PROCEDURE. THE BROKEN TIP DID NOT CONTACT THE PATIENT, AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY. USER FACILITY PERSONNEL CONFIRMED VIA X-RAY THAT THE BROKEN PIECE WAS NOT PRESENT IN THE PATIENT. NO REPORT OF INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22292298 ↗
• InjuryApr 20, 2022Break; Break

  CUSTOMER FILED MEDWATCH # (B)(4). DOCTOR NOTED THE POST OPERATIVE X-RAY A METAL FRAGMENT THAT WAS NOT PART OF THE TOTAL JOINT. THE SURGICAL CAMP WAS FOUND, AND IT WAS MISSING ONE OF THE 3 TEETH. THE PATIENT DECIDED TO UNDERGO ANOTHER SURGERY IN ORDER TO HAVE THE METAL FRAGMENT REMOVED. THE COMPLAINT SAMPLE, PHOTOS, LOT NUMBER, OR FURTHER INFORMATION ARE NOT AVAILABLE.

  Patient problems: Foreign Body In Patient

  MAUDE report 14160590 ↗