Dermacarriers 00-7708-000-10Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00889024375482), received between Dec 21, 2023 and Feb 26, 2025 — classified as 2 injuries, 3 malfunctions.

The most frequently reported specific device problem is “Delivered as Unsterile Product” (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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 26, 2025Patient Device Interaction Problem; Physical Resistance/Sticking; Patient Device Interaction Problem; Physical Resistance/Sticking

  IT WAS REPORTED THAT DURING SURGERY THE CARRIER DID NOT EASILY GO THROUGH THE MESHER, CAUSING THE NORMAL SIZE AND THICKNESS SKIN GRAFT TO BECOME CAUGHT IN THE ROLLER. AN ALTERNATE DEVICE WAS AVAILABLE TO COMPLETE THE PROCEDURE AND AN ADDITIONAL SKIN GRAFT WAS REQUIRED FROM THE PATIENT. NO DELAY TO THE PROCEDURE WAS REPORTED. DILIGENCE IS COMPLETE AND THERE IS NO ADDITIONAL INFORMATION. NO ADDITIONAL CONSEQUENCES HAVE BEEN REPORTED AS A RESULT OF THIS MALFUNCTION.

  Patient problems: Graft failure; Skin Tears

  MAUDE report 21473029 ↗
• MalfunctionJan 16, 2025Delivered as Unsterile Product; Delivered as Unsterile Product

  IT WAS REPORTED THAT DURING INSPECTION THERE WAS HAIR-LIKE SUBSTANCE IN THE PACKAGING. THERE WAS NO PATIENT INVOLVEMENT. DUE DILIGENCE IS COMPLETE AND THERE IS NO ADDITIONAL INFORMATION AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21171985 ↗
• MalfunctionMay 6, 2024Delivered as Unsterile Product; Delivered as Unsterile Product

  IT WAS REPORTED THAT THERE WAS A HAIR LIKE SUBSTANCE DURING INCOMING INSPECTION. THERE IS NO HARM OR DELAY REPORTED. DUE DILIGENCE IS COMPLETE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19249044 ↗
• InjuryMar 27, 2024Material Twisted/Bent; Patient Device Interaction Problem; Material Twisted/Bent; Patient Device Interaction Problem

  IT WAS REPORTED THAT DURING SURGERY THE PRODUCT WAS BREAKING THE SKIN GRAFT AND THERE IS AN ELEVATION ON THE SMOOTH SIDE OF THE CARRIER. AN ALTERNATIVE CARRIER WAS USED TO COMPLETE THE PROCEDURE AND AN UNPLANNED ADDITIONAL SKIN GRAFT WAS TAKEN. THERE WAS NO FURTHER PATIENT IMPACT OR DELAY NOTED. DUE DILIGENCE IS COMPLETE AND THERE IS NO ADDITIONAL INFORMATION AVAILABLE.

  Patient problems: Laceration(s)

  MAUDE report 18986207 ↗
• MalfunctionDec 21, 2023Delivered as Unsterile Product; Delivered as Unsterile Product

  NO ADDITIONAL EVENT INFORMATION AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18372455 ↗