Medline Industries, Inc. DYNJ44929CRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10889942601752), received between Aug 26, 2020 and Aug 26, 2020 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Contamination /Decontamination Problem” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 26, 2020Device Contamination with Chemical or Other Material

  IT WAS REPORTED THAT DURING A CATARACT PROCEDURE, UPON INJECTION FLECKS OF DEBRIS AND SEDIMENT WAS INJECTED INTO THE PATIENT'S EYE.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 10454897 ↗
• MalfunctionAug 26, 2020Contamination /Decontamination Problem

  IT WAS REPORTED THAT DURING A CATARACT PROCEDURE, UPON INJECTION FLECKS OF DEBRIS AND SEDIMENT WAS INJECTED INTO THE PATIENT'S EYE.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 10454606 ↗