Medline Industries, Inc. DYNJRA2366Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10195327642426), received between Oct 4, 2024 and Oct 9, 2024 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Contamination /Decontamination Problem” (4 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.

• MalfunctionOct 9, 2024Contamination /Decontamination Problem; Contamination /Decontamination Problem

  BLACK FLECKS IN THE SYRINGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20407158 ↗
• MalfunctionOct 8, 2024Contamination /Decontamination Problem; Contamination /Decontamination Problem

  ACCORDING TO THE FACILITY ON 09/11/2024 FOREIGN PARTICULATE DESCRIBED AS A BLACK SPECK WAS NOTED INSIDE THE CHAMBER OF THE SYRINGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20401143 ↗
• MalfunctionOct 4, 2024Contamination /Decontamination Problem; Contamination /Decontamination Problem

  ACCORDING TO THE FACILITY ON (B)(6) 2024 FOREIGN PARTICULATE DESCRIBED AS A BLACK SPECK WAS NOTED INSIDE THE CHAMBER OF THE SYRINGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20369134 ↗
• MalfunctionOct 4, 2024Contamination /Decontamination Problem; Contamination /Decontamination Problem

  ACCORDING TO THE FACILITY ON (B)(6) 2024 FOREIGN PARTICULATE DESCRIBED AS A BLACK SPECK WAS NOTED INSIDE THE CHAMBER OF THE SYRINGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20368829 ↗