Medline DYND70664Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10080196813841), received between Jan 30, 2024 and Jan 30, 2024 — classified as 3 injuries.

The most frequently reported specific device problem is “Material Frayed” (3 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 16, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryJan 30, 2024Material Frayed; Material Frayed

  ACCORDING TO THE CUSTOMER, ON 12/29/2023 DURING AN "ENT PROCEDURE", THE GAUZE WAS USED TO APPLY "HIBICLENS" TO THE INCISION SITE "PRIOR TO THE INCISION BEING MADE" AND THE "GAUZED FRAYED".

  Patient problems: Foreign Body In Patient

  MAUDE report 18609158 ↗
• InjuryJan 30, 2024Material Frayed; Material Frayed

  ACCORDING TO THE CUSTOMER, ON (B)(6) 2023 DURING AN "ENT PROCEDURE", THE GAUZE WAS USED TO APPLY "HIBICLENS" TO THE INCISION SITE "PRIOR TO THE INCISION BEING MADE" AND THE "GAUZED FRAYED".

  Patient problems: Foreign Body In Patient

  MAUDE report 18608923 ↗
• InjuryJan 30, 2024Material Frayed; Material Frayed

  ACCORDING TO THE CUSTOMER, ON (B)(6) 2023 DURING AN "ENT PROCEDURE", THE GAUZE WAS USED TO APPLY "HIBICLENS" TO THE INCISION SITE "PRIOR TO THE INCISION BEING MADE" AND THE "GAUZED FRAYED".

  Patient problems: Foreign Body In Patient

  MAUDE report 18608717 ↗