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Mem-Lok RCM-ML3040Recalls & reported problems

Collagen Matrix, Inc. · Resorbable Collagen Membrane for Dental Surgery 30mm x 40mm · Class 2 · Implant

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00813954020761), received between Sep 5, 2018 and Sep 5, 2018 — classified as 1 injury.

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

Device problems

  • Appropriate Device Problem Term/Code Not Available1

Patient problems

  • Unspecified Infection1

Recent adverse event reports

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

  • InjurySep 5, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    THE CLINICIAN REPORTED THAT 10 DAYS FOLLOWING INITIAL DENTAL PROCEDURE A SURGICAL SITE INFECTION WAS OBSERVED AND REQUIRED FOLLOW-UP PROCEDURE TO REMOVE THE MEMBRANE. UPON RE-ENTRY OF THE SURGICAL SITE THE CLINICIAN OBSERVED THAT THE MEMBRANE WAS "GONE". PRIMARY CLOSURE WAS ATTAINED AND SUTURES WERE INTACT PRIOR TO FOLLOW-UP PROCEDURE.

    Patient problems: Unspecified Infection

    MAUDE report 7847186 ↗

Other Barrier, Animal Source, Intraoral devices

All Barrier, Animal Source, Intraoral devices →

Sources and updates

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