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MEMO 3D SMD36Recalls & reported problems

Corcym Srl · 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 08022057013156), received between Feb 8, 2019 and Feb 8, 2019 — 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.

Most reported problems

Device problems

  • Insufficient Device Problem Information1

Patient problems

  • No Information1

Recent adverse event reports

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

  • InjuryFeb 8, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

    BASED ON CAPA (B)(4) INVESTIGATION: THIS EVENT REFERS TO A MEMO 3D SEMIRIGID ANNULOPLASTY RING ICV0972 - # 36 IMPLANTED ON (B)(6) 2015. IT WAS EXPLANTED AND REPLACED WITH A CARBOMEDIS STANDARD PROSTHETIC HEART VALVE, MITRAL M7-033 ON (B)(6) 2016. NO FURTHER EVENT DETAILS WERE PROVIDED.

    Patient problems: No Information

    MAUDE report 8320867 ↗

Other RING, ANNULOPLASTY devices

All RING, ANNULOPLASTY devices →

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