MEMO 3D RECHORD MRCS26Recalls & reported problems
Corcym Srl · Class 2 · Implant
All models of MEMO 3D RECHORD (6)
Data updated Oct 18, 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 08022057015068), received between Jul 28, 2017 and Nov 30, 2018 — classified as 2 injuries.
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
Device problems
- Adverse Event Without Identified Device or Use Problem2
- Appropriate Device Problem Term/Code Not Available1
- Insufficient Device Problem Information1
Patient problems
- No Information2
- Mitral Insufficiency1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryNov 30, 2018Adverse Event Without Identified Device or Use Problem; Appropriate Device Problem Term/Code Not Available; Adverse Event Without Identified Device or Use Problem; Appropriate Device Problem Term/Code Not Available
ON (B)(6) 2018, A MITRAL REPAIR WITH A MEMO3D RECHORD WAS ATTEMPTED. HOWEVER, AFTER THE RING WAS IMPLANTED, IT WAS OBSERVED THAT THE PATIENT'S MITRAL VALVE WAS STILL INCOMPETENT. THEREFORE, THE SURGEON DECIDED TO CONCERT THE REPAIR TO A FULL MITRAL VALVE REPLACEMENT. THE PATIENT DID WELL AFTER SURGERY.
Patient problems: Mitral Insufficiency; No Information
MAUDE report 8121190 ↗InjuryJul 28, 2017Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information
ON (B)(4) 2017 THE MANUFACTURER WAS NOTIFIED THROUGH PATIENT TRACKING OF AN EVENT THAT OCCURRED ON (B)(6), THE INFORMATION RECEIVED TO DATE IS OF A MEMO3D-RECHORD MRCS26 (SN# (B)(4)) THAT WAS IMPLANTED AND EXPLANTED.ON THE SAME DAY.
Patient problems: No Information
MAUDE report 6750864 ↗
Other RING, ANNULOPLASTY devices
- CG FUTURE™ 638BL32Medtronic, Inc. · RING, ANNULOPLASTY1 death71 reports
- PROFILE 3D® 680R28Medtronic, Inc. · RING, ANNULOPLASTY1 death67 reports
- CG FUTURE™ 638BL30Medtronic, Inc. · RING, ANNULOPLASTY1 death65 reports
- CG FUTURE™ 638RL32Medtronic, Inc. · RING, ANNULOPLASTY59 reports
- Tri-Ad™ 900SFC228Medtronic, Inc. · RING, ANNULOPLASTY4 deaths56 reports
- CG FUTURE™ 638BL34Medtronic, Inc. · RING, ANNULOPLASTY51 reports
- Contour 3D® 690R30Medtronic, Inc. · RING, ANNULOPLASTY1 death50 reports
- CG FUTURE™ 638BL28Medtronic, Inc. · RING, ANNULOPLASTY1 death47 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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