Medline Industries, Inc. DYNJRA0676Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10888277810778), received between Apr 21, 2025 and Apr 22, 2025 — classified as 3 malfunctions.

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

• MalfunctionApr 22, 2025Break; Break

  ACCORDING TO THE FACILITY, 3 BROKEN SYRINGES ( 5 CC SYRINGES) WERE DISCOVERED IN 3 SEPARATE KITS ON 3 DIFFERENT DAYS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21882712 ↗
• MalfunctionApr 21, 2025Break; Break

  ACCORDING TO THE FACILITY, 3 BROKEN SYRINGES ( 5 CC SYRINGES) WERE DISCOVERED IN 3 SEPARATE KITS ON 3 DIFFERENT DAYS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21877854 ↗
• MalfunctionApr 21, 2025Break; Break

  ACCORDING TO THE FACILITY, 3 BROKEN SYRINGES ( 5 CC SYRINGES) WERE DISCOVERED IN 3 SEPARATE KITS ON 3 DIFFERENT DAYS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21877853 ↗