MEMO 3D SMD26Recalls & reported problems
Corcym Srl · Class 2 · Implant
- 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 08022057013101), received between Nov 2, 2017 and Jun 19, 2022 — classified as 7 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (7 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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Insufficient Device Problem Information7
- Adverse Event Without Identified Device or Use Problem2
Patient problems
- Insufficient Information4
- No Information3
- No Known Impact Or Consequence To Patient2
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
InjuryJun 19, 2022Insufficient Device Problem Information; Insufficient Device Problem Information
THE MANUFACTURER WAS INFORMED OF THE FOLLOWING EVENT THROUGH PATIENT TRACKING DEPARTMENT. BASED ON THE INFORMATION ON THE PATIENT'S IMPLANT FORM, ON (B)(6) 2022, MEMO 3D SEMIRIGID ANNULOPLASTY RING SMD26 WAS IMPLANTED AND EXPLANTED INTRA-OPERATIVELY. NO ALLEGATION OF DEVICE MALFUNCTION NOR SERIOUS INJURY ON THE PATIENT HAS BEEN RECEIVED FROM THE HOSPITAL REGARDING THIS EVENT.
Patient problems: Insufficient Information
MAUDE report 14740345 ↗InjuryJun 19, 2022Insufficient Device Problem Information; Insufficient Device Problem Information
THE MANUFACTURER WAS INFORMED OF THE FOLLOWING EVENT THROUGH PATIENT TRACKING DEPARTMENT. BASED ON THE INFORMATION ON THE PATIENT'S IMPLANT FORM, ON (B)(6) 2022, MEMO 3D SEMIRIGID ANNULOPLASTY RING SMD26 WAS IMPLANTED AND EXPLANTED INTRA-OPERATIVELY. NO ALLEGATION OF DEVICE MALFUNCTION NOR SERIOUS INJURY ON THE PATIENT HAS BEEN RECEIVED FROM THE HOSPITAL REGARDING THIS EVENT.
Patient problems: Insufficient Information
MAUDE report 14740344 ↗InjuryMay 27, 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 SEMIRIGID ANNULOPLASTY RING SMD26 WAS IMPLANTED AND EXPLANTED ON (B)(6) 2021. ANOTHER SIMILAR DEVICE SMD26 WAS FINALLY IMPLANTED. 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 11898619 ↗InjuryMay 27, 2021Insufficient Device Problem Information; Insufficient Device Problem Information
InjuryNov 21, 2018Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information
IT WAS REPORTED THAT A MEMO3D SIZE 26 WAS IMPLANTED AND EXPLANTED INTRAOPERATIVELY. NO OTHER INFORMATION WAS PROVIDED.
Patient problems: No Information; No Known Impact Or Consequence To Patient
MAUDE report 8097954 ↗InjuryApr 26, 2018Adverse 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)(6) , 2018 A MEMO 3D SMD26 SEMIRIGID ANNULOPLASTY MITRAL REPAIR RING WAS IMPLANTED. THE MANUFACTURER RECEIVED A NOTIFICATION THAT THE VALVE WAS EXPLANTED THE SAME DAY AND REPLACED WITH A MEMO 3D SMD28 REPAIR RING.
Patient problems: No Information; No Known Impact Or Consequence To Patient
MAUDE report 7465669 ↗InjuryNov 2, 2017Insufficient Device Problem Information; Insufficient Device Problem Information
ON (B)(6) 2017 THE MANUFACTURER WAS NOTIFIED THROUGH PATIENT TRACKING OF A MEMO3D #28 THAT WAS IMPLANTED ON (B)(6) 2017. PATIENT TRACKING WAS PREVIOUSLY AWARE OF A MEMO3D #26 THAT WAS IMPLANTED IN THE SAME PATIENT ON (B)(6) 2017.
Patient problems: No Information
MAUDE report 6997871 ↗
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™ 638RL30Medtronic, Inc. · RING, ANNULOPLASTY1 death47 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.