Medline Industries, Inc. DYNJ81802ARecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10195327359638), received between Mar 18, 2024 and Mar 18, 2024 — 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 18, 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.

• MalfunctionMar 18, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE FACILITY ON 02/27/24 THE "NEEDLE WAS PUT ON SYRINGE AND HANDED TO DOCTOR TO INJECT, AS SOON AS THE DOCTOR PUSHED ON SYRINGE THE NEEDLE FLEW OFF".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18921433 ↗
• MalfunctionMar 18, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE FACILITY ON (B)(6) 2024 THE "NEEDLE WAS PUT ON SYRINGE AND HANDED TO DOCTOR TO INJECT, AS SOON AS THE DOCTOR PUSHED ON SYRINGE THE NEEDLE FLEW OFF".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18921201 ↗