Mem-Lok RCM-ML1520Recalls & reported problems
Collagen Matrix, Inc. · Resorbable Collagen Membrane for Dental Surgery 15mm x 20mm · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00813954020747), received between Mar 3, 2026 and Mar 3, 2026 — classified as 2 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information2
Patient problems
- Unspecified Infection2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMar 3, 2026Insufficient Device Problem Information
A COMPLAINT REGARDING MEM-LOK RESORBABLE COLLAGEN MEMBRANE STATING "GRAFT FAILED AT IMPLANT SITE #6, #7, AND #8 DUE TO INFECTION. PATIENT CARE RESOLVED BY INSERTING A NEW GRAFT". NO OTHER INFORMATION REGARDING PATIENT STATUS HAS BEEN PROVIDED.
Patient problems: Unspecified Infection
MAUDE report 24497510 ↗InjuryMar 3, 2026Insufficient Device Problem Information
A COMPLAINT REGARDING MEM-LOK RESORBABLE COLLAGEN MEMBRANE STATING "GRAFT FAILED AT IMPLANT SITE #12 AND #31 DUE TO INFECTION. PATIENT CARE RESOLVED BY INSERTING A NEW GRAFT". NO OTHER INFORMATION REGARDING PATIENT STATUS HAS BEEN PROVIDED.
Patient problems: Unspecified Infection
MAUDE report 24497508 ↗
Other Barrier, Animal Source, Intraoral devices
- GIBSON HEALTHCARE 5303-235Benco Dental Supply CO. · Barrier, Animal Source, Intraoral2 recalls0 reports
- GIBSON HEALTHCARE 5303-306Benco Dental Supply CO. · Barrier, Animal Source, Intraoral1 recall0 reports
- Neomem N1520Collagen Matrix, Inc. · Barrier, Animal Source, Intraoral1 recall0 reports
- GIBSON HEALTHCARE 5303-342Benco Dental Supply CO. · Barrier, Animal Source, Intraoral1 recall0 reports
- GIBSON HEALTHCARE 5303-324Benco Dental Supply CO. · Barrier, Animal Source, Intraoral1 recall0 reports
- GIBSON HEALTHCARE 5303-226Benco Dental Supply CO. · Barrier, Animal Source, Intraoral1 recall0 reports
- BioMend 0103ZCollagen Matrix, Inc. · Barrier, Animal Source, Intraoral4 reports
- SYMBIOS® USOSCRM1520Dentsply Implants Manufacturing GmbH · Barrier, animal source, intraoral3 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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