RCT Resorbable Collagen Tape 5091000Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00614950007233), received between Feb 28, 2020 and Feb 28, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 28, 2020Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information

  THE DOCTOR STATED THAT THE PATIENTS, WHO HAD COLLAGEN TAPE PLACED, HAD DRY SOCKETS WITH GREY PURULENT MATERIAL. ONE PATIENT HAD MULTIPLE EXTRACTIONS AND DEVELOPED DRY SOCKET/INFECTION IN THE UPPER QUADRANT WHERE THEY PLACED THE COLLAGEN TAPE. DRY SOCKET PACKS WERE PLACED TO CIRCUMVENT THIS COMPLICATION. THERE WAS NO DELAY IN HEALING OR PATIENT INJURY REPORTED.

  Patient problems: No Code Available; Unspecified Infection

  MAUDE report 9771255 ↗