Skip to content

Socket Repair Membrane 0154Recalls & reported problems

Collagen Matrix, Inc. · Absorbable Collagen Membrane 10mm x 20mm · Class 2 · Implant

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 00813954020464), received between Jun 25, 2025 and Jun 25, 2025 — 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. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 1 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Insufficient Device Problem Information1

Patient problems

  • Insufficient Information1

Recent adverse event reports

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

  • InjuryJun 25, 2025Insufficient Device Problem Information; Insufficient Device Problem Information

    COMPLAINT SUBMITTED THROUGH CLINICAL LITERATURE SEARCH REVIEW. LIMITED INFORMATION PROVIDED AND IT IS UNLIKELY FURTHER INFORMATION SURROUNDING THE PATIENT OR EVENT WILL BE PROVIDED. PRODUCT PART OF THE CLINICAL LITERATURE SEARCH IS SOCKET REPAIR MEMBRANE. NO LOT NUMBER OR ITEM NUMBER WAS SPECIFIED. THIS SINGLE COMPLAINT WAS REPORTED WITH MULTIPLE EVENTS. TITLE OF THE LITERATURE: BECK, T. M., & MEALEY, B. L. (2010). HISTOLOGIC ANALYSIS OF HEALING AFTER TOOTH EXTRACTION WITH RIDGE PRESERVATION USING MINERALIZED HUMAN BONE ALLOGRAFT. JOURNAL OF PERIODONTOLOGY, 81(12), 1765-1772. FROM THE ARTICLE, ONE SITE IN THE EARLY HEALING GROUP AND TWO SITES IN THE DELAYED HEALING GROUP PRESENTED WITH SIGNS OF POTENTIAL INFECTION AT THE 7- TO 10-DAY POSTOPERATIVE FOLLOW-UP. NO FURTHER INFORMATION SURROUNDING PATIENT STATUS OR PATIENT OUTCOME WAS PROVIDED. THE BACKGROUND OF THE STUDY BY BECK AND MEALEY (2010) INVESTIGATED BONE HEALING AFTER TOOTH EXTRACTION WHEN RIDGE PRESERVATION WAS PERFORMED USING MINERALIZED HUMAN BONE ALLOGRAFT. THE BACKGROUND HIGHLIGHTS THAT SIGNIFICANT ALVEOLAR BONE LOSS TYPICALLY FOLLOWS EXTRACTION, AND RIDGE PRESERVATION AIMS TO MITIGATE THIS. THE RESEARCHERS COMPARED HEAL

    Patient problems: Insufficient Information

    MAUDE report 22326930 ↗

Other Barrier, Animal Source, Intraoral devices

All Barrier, Animal Source, Intraoral devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.