Medline Industries, Inc. DYNJ51729BRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10193489285161), received between Jun 6, 2023 and Jun 21, 2023 — classified as 2 injuries.

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

• InjuryJun 21, 2023Material Integrity Problem; Material Integrity Problem

  ACCORDING TO THE CUSTOMER, DURING A "LEFT BREAST-NEEDLE LOCALIZED EXCISIONAL BIOPSY" THE RAYTEC WAS BEING USED TO "ADDRESS BLEEDING" AND FRAYED INSIDE THE PATIENT.

  Patient problems: Foreign Body In Patient

  MAUDE report 17175096 ↗
• InjuryJun 6, 2023Material Integrity Problem; Material Integrity Problem

  ACCORDING TO THE FACILITY ON (B)(6) 2023 DURING A PROCEDURE "RAYTEC FRAYED AND MD HAD TO PICK A PIECE OUT OF THE PATIENT'S INCISION".

  Patient problems: Foreign Body In Patient

  MAUDE report 17075403 ↗