Medline Industries, Inc. DYND70760Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10080196853236), received between Jun 19, 2019 and Jun 19, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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.

• MalfunctionJun 19, 2019Detachment of Device or Device Component

  IT WAS REPORTED THAT DURING PREP FOR A DILATATION AND CURETTAGE, THE SPONGE STICK CAME OFF THE SPONGE AND SPONGE WAS STUCK IN THE PATIENT'S VAGINA.

  Patient problems: No Code Available; No Known Impact Or Consequence To Patient

  MAUDE report 8712991 ↗