Medline Industries, Inc. DYKC1586Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10193489472837), received between Apr 1, 2021 and Apr 1, 2021 — classified as 1 injury.

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryApr 1, 2021Device Slipped; Device Contamination with Chemical or Other Material

  IT WAS REPORTED THAT THE PATIENT WAS UNDERGOING A SCHEDULED DAVINCI BILATERAL INGUINAL HERNIA REPAIR THAT WAS CONVERTED FROM A ROBOTIC TO A LAPAROSCOPIC HERNIA REPAIR WHEN THE PATIENT WAS FOUND SHIFTED OFF OF THE BED ABOUT 2 INCHES CAUSING THE DAVINCI ARM TO EXIT ONE OF THE ABDOMINAL INCISIONS AND THE STERILE FIELD WAS CONTAMINATED.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 11603096 ↗