Medline Industries, Inc. DYNJ85700ARecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10198459326837), received between Aug 12, 2026 and Aug 12, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Twisted/Bent” (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 16, 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.

• MalfunctionAug 12, 2026Unraveled Material; Material Twisted/Bent

  It was reported that Techs report they had the fuzzies from the blue towel issue on the IR pack at the end of last week. The fuzz gets into the plastic trays for water and mixes with the water making it unusable.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50220794 ↗