MEDLINE DYNJLHH2Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 80080196761844), received between Sep 24, 2026 and Sep 24, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Unsealed Device Packaging” (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. How this data works · Data updated Oct 13, 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.

• MalfunctionSep 24, 2026Unsealed Device Packaging

  This VMSR report summarizes 1 malfunction event involving DYNJLHH2. The account reported that the item was not sealed correctly and therefore was not sterile. Evaluation of five returned samples confirmed that the items were not properly sealed. Based on the complaint details, sample evaluation, and investigation, the reported issue was confirmed. No patient information was available. No patient or user injuries were reported.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50888574 ↗