Medline Industries, Inc. DYNJ907722BRecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10195327129262), received between Nov 8, 2022 and Aug 11, 2026 — classified as 3 injuries, 1 malfunction.

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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 11, 2026Material Frayed

  It was reported that fraying gauze was found. We just received another pack of Raytecs that were fraying and coming apart.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50209229 ↗
• InjuryMay 31, 2023Material Integrity Problem; Material Integrity Problem

  PER THE FACILITY GAUZE FIBERS ARE FALLING OFF INTO THE PATIENT CAVITY DURING SURGERY.

  Patient problems: Foreign Body In Patient

  MAUDE report 17033125 ↗
• InjuryDec 21, 2022Material Integrity Problem; Material Integrity Problem

  GAUZE FELL APART DURING PROCEDURE AND NEEDED TO BE REMOVED FROM THE PATIENT.

  Patient problems: Foreign Body In Patient

  MAUDE report 16023398 ↗
• InjuryNov 8, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE FACILITY THE LAP SPONGES WERE FALLING APART AND LEAVING BEHIND STRINGS IN THE WOUND THAT HAD TO BE REMOVED DURING SURGERY.

  Patient problems: Foreign Body In Patient

  MAUDE report 15754481 ↗