Medline Industries, Inc. DYNJ0516998IRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10889942072262), received between May 11, 2018 and May 14, 2018 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Break” (2 reports).

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.

• MalfunctionMay 14, 2018Break

  IT WAS REPORTED THAT IN THE MIDDLE OF AN UNKNOWN ORTHOPEDIC PROCEDURE, THE YANKAUER TIP BROKE OFF INTO SURGICAL SITE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7511468 ↗
• InjuryMay 11, 2018Break; Component Falling

  IT WAS REPORTED THAT DURING A LEFT TOTAL SHOULDER PROCEDURE, THE YANKAUER TIP BROKE OFF AND FELL INTO THE SURGICAL SITE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7507107 ↗