Medline Industries, Inc. DYND70670Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10080196464982), received between Aug 11, 2026 and Sep 29, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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.

• MalfunctionSep 29, 2026Device Contamination with Chemical or Other Material; Packaging Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50935411 ↗
• MalfunctionAug 11, 2026Unsealed Device Packaging

  It was reported that The bag isn¿t sealed so it¿s not sterile.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50210843 ↗