Medline Industries, Inc. DYNJ04079ZRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10080196819256), received between Feb 23, 2023 and Feb 23, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Dull, Blunt” (1 report).

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 23, 2023Product Quality Problem; Dull, Blunt; Product Quality Problem; Dull, Blunt

  ACCORDING TO THE FACILITY ON (B)(6) 2023 DURING A CIRCUMCISION THE "CLINICIAN CLAIMED THE BLADE IN THE KIT WASN'T CUTTING PROPERLY AND NOTED THE SCALPEL WAS BLUNT, WHICH CAUSED TRAUMA TO THE CUT AREA REQUIRING THE CLINICIAN TO USE GEL FOAM TO STOP THE BLEEDING."

  Patient problems: Genital Bleeding

  MAUDE report 16428109 ↗