Medline Industries, Inc. DYNJS0310Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10080196942589), received between Nov 14, 2023 and Nov 14, 2023 — classified as 1 injury.

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

1. Mar 3, 2025Class IIOpen, Classified

   There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

   Z-1598-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

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.

• InjuryNov 14, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE FACILITY ON (B)(6) 2023 "THE RAYTEC WAS BEING USED TO STOP A BLEEDING AREA ON A LAPAROSCOPIC CASE WITHIN THE ABDOMEN BEING HELD BY A LAPAROSCOPIC GRASPER".

  Patient problems: Foreign Body In Patient

  MAUDE report 18133700 ↗