Medline Industries, Inc. DYNDF1072ARecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10884389542040), received between Apr 23, 2021 and Aug 18, 2021 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Mechanical Problem” (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 18, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 18, 2021Flaked

  DURING CIRCUMCISION, METAL SHAVINGS FLAKED OFF THE HEMOSTATS, FROM MEDLINE INDUSTRIES, INC. CIRCUMCISION TRAY, TO THE PATIENT DURING A STERILE PROCEDURE.

  Patient problems: Foreign Body In Patient

  MAUDE report 12335830 ↗
• MalfunctionApr 26, 2021Mechanical Problem; Defective Device; Material Integrity Problem

  HEALTH CARE PROVIDER REPORTED HEMOSTAT DID NOT CLAMP CORRECTLY, THERE WAS A GAP IN THE INSTRUMENT.

  Patient problems: Insufficient Information

  MAUDE report 11723433 ↗
• MalfunctionApr 23, 2021Mechanical Problem

  HEALTH CARE PROVIDER REPORTED HEMOSTAT DID NOT CLAMP CORRECTLY. THERE WAS A GAP IN THE INSTRUMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11715622 ↗
• MalfunctionApr 23, 2021Dull, Blunt

  SCISSORS, FROM MEDLINE CIRCUMCISION TRAY, REPORTED AS DULL PER PEDIATRICIAN.

  Patient problems: Insufficient Information

  MAUDE report 11715621 ↗