MEMO 3D RECHORD MRCS34Recalls & 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
- 7
- Deaths reported
- 0
- Injuries reported
- 7
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 08022057015105), received between Aug 10, 2017 and May 12, 2022 — classified as 7 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (5 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 18, 2026.
Most reported problems
Device problems
- Insufficient Device Problem Information5
- Adverse Event Without Identified Device or Use Problem4
- Inadequacy of Device Shape and/or Size1
Patient problems
- Insufficient Information3
- No Information3
- Mitral Regurgitation1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
InjuryMay 12, 2022Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information
THE MANUFACTURER WAS INFORMED OF THIS EVENT THROUGH THE DEVICE TRACKING DEPARTMENT. BASED ON THE INFORMATION REPORTED ON THE PATIENT IMPLANT FORM, A MEMO 3D RECHORD SEMIRIGID ANNULOPLASTY RING MRCS34 WAS IMPLANTED AND EXPLANTED ON (B)(6) 2022. THE MANUFACTURER HAS NOT RECEIVED FROM THE SITE ANY ALLEGATION OF A DEVICE MALFUNCTION NOR OF SERIOUS INJURY REGARDING THIS EVENT.
Patient problems: Insufficient Information
MAUDE report 14376232 ↗InjuryJun 18, 2021Insufficient Device Problem Information; Insufficient Device Problem Information
THE MANUFACTURER WAS INFORMED OF THIS EVENT THROUGH THE DEVICE TRACKING DEPARTMENT. BASED ON THE INFORMATION REPORTED IN THE PATIENT IMPLANT FORM, A MEMO 3D RECHORD SEMIRIGID ANNULOPLASTY RING MRCS34 WAS IMPLANTED ON (B)(6) 2020. THE DEVICE WAS EXPLANTED ON (B)(6) 2021 AND REPLACED WITH A NEW MRCS34. NO FURTHER INFORMATION IS PRESENTLY AVAILABLE. NO ALLEGATION OF A DEVICE MALFUNCTION NOR OF A SERIOUS INJURY WAS RECEIVED FROM THE SITE REGARDING THIS EVENT.
Patient problems: Insufficient Information
MAUDE report 12025772 ↗InjuryJun 17, 2021Insufficient Device Problem Information; Insufficient Device Problem Information
THE MANUFACTURER WAS INFORMED OF THIS EVENT THROUGH THE DEVICE TRACKING DEPARTMENT. BASED ON THE INFORMATION REPORTED IN THE PATIENT IMPLANT FORM, A MEMO 3D RECHORD SEMIRIGID ANNULOPLASTY RING MRCS34 WAS IMPLANTED ON (B)(6) 2020. THE DEVICE WAS EXPLANTED ON (B)(6) 2021 AND REPLACED WITH A NEW MRCS34. NO FURTHER INFORMATION IS PRESENTLY AVAILABLE. NO ALLEGATION OF A DEVICE MALFUNCTION NOR OF A SERIOUS INJURY WAS RECEIVED FROM THE SITE REGARDING THIS EVENT.
Patient problems: Insufficient Information
MAUDE report 12021788 ↗InjuryOct 16, 2019Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information
A PATIENT WAS INTENDED TO RECEIVE A MEMO3D-RECHORD #34 ON (B)(6) 2019. THE MANUFACTURER WAS NOTIFIED THE DEVICE WAS IMPLANTED AND EXPLANTED ON THE SAME DAY. NO FURTHER INFORMATION WAS RECEIVED.
Patient problems: No Information
MAUDE report 9199763 ↗InjuryOct 16, 2019Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information
A PATIENT WAS INTENDED TO RECEIVE A MEMO3D-RECHORD #34 ON (B)(6) 2019. THE MANUFACTURER WAS NOTIFIED THE DEVICE WAS IMPLANTED AND EXPLANTED ON THE SAME DAY. NO FURTHER INFORMATION WAS RECEIVED.
Patient problems: No Information
MAUDE report 9199736 ↗InjuryNov 8, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT A MEMO3D RECHORD, SIZE 34, WAS IMPLANTED AND EXPLANTED INTRA-OPERATIVELY ON (B)(6) 2018. NO OTHER INFORMATION WAS PROVIDED.
Patient problems: No Information
MAUDE report 8052366 ↗InjuryAug 10, 2017Inadequacy of Device Shape and/or Size; Inadequacy of Device Shape and/or Size
ON (B)(6) 2017 THE MANUFACTURER WAS NOTIFIED THROUGH PATIENT TRACKING OF A MEMO 3D RECHORD SEMIRIGID ANNULOPLASTY RING THAT WAS IMPLANTED/EXPLANTED ON (B)(6) 2017. FURTHER INFORMATION FROM THE PHYSICIAN INFORMED THE MANUFACTURER THAT THE RING WAS IMPLANTED ON (B)(6), DURING THE PROCEDURE WHEN THE PATIENT WAS COMING OFF THE PUMP, SYSTOLIC ANTERIOR MOTION (SAM) ON ECHO WAS OBSERVED. THE PHYSICIAN DECIDED TO PUT THE PATIENT BACK ON PUMP AND EXPLANT THE DEVICE. A MEDTRONIC CG FUTURE BAND SIZE 36 WAS THEN IMPLANTED. THE PATIENT IS DOING WELL FOLLOWING THE SURGERY. AN ADDITIONAL X CLAMP TIME OF APPROX 20-30 MINUTES WAS ADDED TO THE PROCEDURE.
Patient problems: Mitral Regurgitation
MAUDE report 6786835 ↗
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.
How reports and recalls are matched · Editorial policy · Report an error on this page