MEMO 3D RECHORDRecalls & reported problems across all models
Corcym Srl · 6 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 36
- Deaths reported
- 2
- Injuries reported
- 33
- Recalls
- 0
We found 6 models of MEMO 3D RECHORD by Corcym Srl in the FDA's device registry (GUDID). Together they are named in 36 adverse event reports in the FDA's MAUDE database, received between Dec 2, 2016 and May 12, 2022 — classified as 2 deaths, 33 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (18 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Most reported MEMO 3D RECHORD problems
Device problems
- Insufficient Device Problem Information18
- Adverse Event Without Identified Device or Use Problem15
- Detachment of Device or Device Component7
- Leak/Splash2
- Appropriate Device Problem Term/Code Not Available1
- Inadequacy of Device Shape and/or Size1
- Malposition of Device1
- Material Deformation1
Patient problems
- No Information17
- Insufficient Information7
- Dyspnea5
- Mitral Regurgitation4
- Mitral Insufficiency3
- Fatigue2
- No Known Impact Or Consequence To Patient2
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
MEMO 3D RECHORD models
6 models, most reported first. Each model has its own page with its reports, recalls and device details.
- MEMO 3D RECHORD MRCS32RING, ANNULOPLASTY1 death11 reports
- MEMO 3D RECHORD MRCS28RING, ANNULOPLASTY9 reports
- MEMO 3D RECHORD MRCS34RING, ANNULOPLASTY7 reports
- MEMO 3D RECHORD MRCS30RING, ANNULOPLASTY1 death5 reports
- MEMO 3D RECHORD MRCS26RING, ANNULOPLASTY2 reports
- MEMO 3D RECHORD MRCS38RING, ANNULOPLASTY2 reports
Recent MEMO 3D RECHORD adverse event reports
The 15 most recent reports across all models, 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 ↗InjuryApr 12, 2022Insufficient Device Problem Information; Insufficient Device Problem Information
THE MANUFACTURER WAS INFORMED ON THIS EVENT THROUGH THE DEVICE TRACKING DEPARTMENT. BASED ON THE INFORMATION REPORTED ON THE PATIENT IMPLANT FORM, A MEMO 3D RECORD SEMIRIGID ANNULOPLASTY RING MRCS32 WAS IMPLANTED AND EXPLANTED ON (B)(6) 2021. THE DEVICE WAS REPORTEDLY WASTED. THE MANUFACTURER HAS NOT RECEIVED ANY ALLEGATION OF A DEVICE MALFUNCTION NOR OF SERIOUS INJURY FROM THE SITE REGARDING THIS EVENT.
Patient problems: Insufficient Information
MAUDE report 14089214 ↗InjurySep 29, 2021Insufficient Device Problem Information; Insufficient Device Problem Information
THE MANUFACTURE WAS INFORMED OF THE EVENT THROUGH THE PATIENT TRACKING DEPARTMENT. BASED ON THE INFORMATION REPORTED IN THE PATIENT IMPLANT FORM, A MEMO 3D RECHORD #30 VALVE WAS IMPLANTED AND EXPLANTED ON THE SAME DAY ON (B)(6) 2021. NO FURTHER INFORMATION ABOUT ANY DEVICE MALFUNCTION, PATIENT OUTCOME OR DEVICE FINALLY IMPLANTED WAS RECEIVED FROM THE SITE REGARDING THIS EVENT.
Patient problems: Insufficient Information
MAUDE report 12551106 ↗InjurySep 29, 2021Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information
THE MANUFACTURE WAS INFORMED OF THE EVENT THROUGH THE PATIENT TRACKING DEPARTMENT. BASED ON THE INFORMATION REPORTED IN THE PATIENT IMPLANT FORM, A MEMO 3D RECHORD #30 VALVE WAS IMPLANTED AND EXPLANTED ON THE SAME DAY ON (B)(6) 2021. NO FURTHER INFORMATION ABOUT ANY DEVICE MALFUNCTION, PATIENT OUTCOME OR DEVICE FINALLY IMPLANTED WAS RECEIVED FROM THE SITE REGARDING THIS EVENT. THE MANUFACTURER OBTAINED ADDITIONAL INFORMATION IDENTIFYING THAT THE RING WAS EXPLANTED DUE TO A FAILED COMPLEX MITRAL VALVE REPAIR. THE EVENT WAS DEEMED NOT DEVICE RELATED BASED ON THE SURGEON'S ASSESSMENT.
Patient problems: Insufficient Information
MAUDE report 12551097 ↗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 ↗InjuryJun 11, 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 SIZE 32 WAS IMPLANTED ON (B)(6) 2019. IT WAS EXPLANTED ON (B)(6)2021 AND REPLACED WITH A CARBOMEDICS OPTIFORM MITRAL HEART VALVE F7-029. 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: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 11982135 ↗InjuryJun 8, 2021Perivalvular Leak; Detachment of Device or Device Component; Insufficient Device Problem Information; Perivalvular Leak; Detachment of Device or Device Component; 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 SIZE 32 WAS IMPLANTED ON (B)(6) 2019. IT WAS EXPLANTED ON (B)(6) 2021 AND REPLACED WITH A CARBOMEDICS OPTIFORM MITRAL HEART VALVE F7-029. BASED ON THE ADDITIONAL INFORMATION RECEIVED FROM THE OPERATIONAL REPORT, THE PATIENT PRESENTED PREVIOUS MITRAL VALVE STENOSIS AND INSUFFICIENCY AFTER PRIOR MITRAL VALVE AND HAD UNDERGONE A TRANSCATHETER MITRAL VALVE ( EDWARDS TRANSCATHETER VALVE LEADING TO A PARAVALVULAR LEAK). THE ANNULUS OF THE PREVIOUS ANNULOPLASTY RING HAD PULLED AWAY FROM THE POSTERIOR LEAFLET RESULTING IN A PARAVALVULAR LEAK. THE EDWARDS TRANSCATHETER VALVE AND THE MEMO 3D RING WERE EXPLANTED ON (B)(6) 2021 AND REPLACED WITH A CARBOMEDICS OPTIFORM MITRAL HEART VALVE F7-029. THE PATIENTS MEDICAL HISTORY INCLUDES HODGKIN DISEASE, ACUTE-ON-CHRONIC CONGESTIVE HEART FAILURE, HYPERLIPIDEMIA, TRANSCATHETER MITRAL VALVE IN MITRAL VALVE RING ANNULUS AND CHRONIC OBSTRUCTIVE PULMONARY DISEASE. PATIENT WAS RETURNED TO ICU IN A STABLE CONDITION AND THEIR DISCHARGE CONDITION WAS GOOD. BASED ON INF
Patient problems: Insufficient Information; Mitral Valve Insufficiency/ Regurgitation; Mitral Valve Stenosis
MAUDE report 11962515 ↗InjuryApr 11, 2020Leak/Splash; Leak/Splash
ON (B)(6) 2020 A PATIENT RECEIVED A MEMO-3D RECHORD MECHANICAL RING AS PART OF AN MITRAL VALVE REPAIR. THE MANUFACTURER WAS NOTIFIED THAT MITRAL REGURGITATION WAS OBSERVED, AND THE SITE RECOMMENDED RE-VALVULOPLASTY HOWEVER THE PATIENT WANTED TO REPLACE THE VALVE. ON (B)(6) 2020, MEMO 3D WAS EXPLANTED AND EPIC (29MM) WAS IMPLANTED. PATIENT WAS IN GOOD CONDITION AFTER OPERATION. NO FURTHER INFORMATION WAS RECEIVED.
Patient problems: Mitral Regurgitation
MAUDE report 9951720 ↗InjuryApr 11, 2020Leak/Splash; Leak/Splash
ON (B)(6) 2020 A PATIENT RECEIVED A MEMO-3D RECHORD MECHANICAL RING AS PART OF AN MITRAL VALVE REPAIR. THE MANUFACTURER WAS NOTIFIED THAT MITRAL REGURGITATION WAS OBSERVED, AND THE SITE RECOMMENDED RE-VALVULOPLASTY HOWEVER THE PATIENT WANTED TO REPLACE THE VALVE. ON (B)(6) 2020, MEMO 3D WAS EXPLANTED AND EPIC (29MM) WAS IMPLANTED. PATIENT WAS IN GOOD CONDITION AFTER OPERATION. NO FURTHER INFORMATION WAS RECEIVED.
Patient problems: Mitral Regurgitation
MAUDE report 9951718 ↗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 #32 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 9199904 ↗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 #32 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 9199881 ↗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 ↗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 #28 ON (B)(6) 2019. THE MANUFACTURER WAS NOTIFIED THE DEVICE WAS IMPLANT/ED AND EXPLANTED ON THE SAME DAY. NO FURTHER INFORMATION WAS RECEIVED.
Patient problems: No Information
MAUDE report 9198587 ↗
Other Corcym Srl products
- CARBOMEDICS SUPRA-ANNULAR (TOP HAT)5 models · 99 reports
- PERCEVAL PLUS4 models · 92 reports
- CARBOMEDICS STANDARD12 models · 83 reports
- MEMO 3D7 models · 54 reports
- CARBOMEDICS ANNULOFLEX6 models · 53 reports
- CARBOMEDICS REDUCED6 models · 39 reports
- CARBOMEDICS OPTIFORM6 models · 37 reports
- Memo 4D7 models · 29 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page