MEDLINE DYNJTS4306Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10889942602261), received between Mar 3, 2026 and Mar 3, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Separation” (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.

• MalfunctionMar 3, 2026Material Separation

  LUMBAR DRAIN WAS BEING REMOVED IN STANDARD PROCEDURE WITH THE PATIENT IN LATERAL DECUBITUS POSITION. LUMBAR DRAIN DID NOT HAVE ANY RESISTANCE BUT AT THE END SNAPPED AND BROKE OFF TIP WITHIN THE SOFT TISSUE OF THE PATIENT'S BODY. NO PAIN BY THE PATIENT.

  Patient problems: Foreign Body In Patient

  MAUDE report 24501583 ↗