HENRY SCHEIN 5700741Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00304040064375), received between Oct 4, 2024 and Jan 19, 2025 — classified as 2 malfunctions.

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

• MalfunctionJan 19, 2025No Apparent Adverse Event; No Apparent Adverse Event

  THIS VMSR REPORT SUMMARIZES ONE MALFUNCTION EVENT. DOCTOR STATES THAT THE HANDPICE (B)(4) DOES NOT HOLD THE BURS SHE IS USING TO TREAT PATIENT. SHE IS UNABLE TO PUSH THEM IN, THEREFORE, WHEN SHE TREATS PATIENTS THE BURS FALL OUT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21188244 ↗
• MalfunctionOct 4, 2024No Apparent Adverse Event; No Apparent Adverse Event

  DOCTOR STATES THAT THE HANDPICES DOES NOT HOLD THE BURS SHE IS USING TO TREAT PATIENT. SHE IS UNABLE TO PUSH THEM IN, THEREFORE, WHEN SHE TREATS PATIENTS THE BURS FALL OUT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20378505 ↗