MEMO 3D RECHORD MRCS38Recalls & 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 08022057015129), received between Jul 7, 2017 and Dec 6, 2017 — classified as 2 injuries.
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
Patient problems
- Dyspnea1
- Mitral Regurgitation1
- No Information1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryDec 6, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A MITRAL ANNULOPLASTY THAT DID NOT REQUIRE WORK ON THE CHORDAE WAS PERFORMED USING A MEMO 3D RECHORD. AFTER POSITIONING THE RING, THE PHYSICIAN WAS UNABLE TO PULL THE BLUE STRING TO RELEASE THE YELLOW GUIDING SUTURE ON THE RING. THE SURGERY WAS COMPLETED AND THE YELLOW SUTURE WAS LEFT IN PLACE. NO NEGATIVE PATIENT IMPACT WAS REPORTED, AND THE DEVICES FUNCTIONALITY WAS REPORTED TO BE UNAFFECTED BY THE EVENT.
Patient problems: No Information
MAUDE report 7089269 ↗InjuryJul 7, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE PATIENT HAD MINIMALLY INVASIVE MITRAL VALVE REPAIR USING A SMALL RIGHT THORACOTOMY. THIS REPAIR CONSISTED OF GORE-TEX NEOCHORDAE PLACED TO THE A2 AND P2 SCALLOPS OF THE ANTERIOR AND POSTERIOR MITRAL VALVE LEAFLETS SUPPLEMENTED WITH A 38MM MEMO 3D RECHORD ANNULOPLASTY RING. COMPLETION TRANSESOPHAGEAL ECHO AT THE TIME REVEALED A WELL SEATED BAND. A FOLLOW UP TTE AT THE 3 WEEK MARK SHOWED A STABLE MITRAL REPAIR. FURTHER TTE 2 WEEKS LATER REVEALED A ROCKING ANNULOPLASTY BAND. PATIENT RETURNED TO OPERATING ROOM AND IT WAS DETERMINED THAT APPROXIMATELY TWO THIRDS OF THE CIRCUMFERENCE OF THE PRIOR ANNULOPLASTY BAND HAD DEHISCED COMPLETELY FROM THE MITRAL VALVE ANNULUS. THE SUTURE TECHNIQUE USED BY THE PHYSICIAN FOR MEMO 3D RECHORD IS ETHIBOND 3.0 INTERRUPTED MATTRESS SUTURES, TIED WITH COR-NOT. .
Patient problems: Dyspnea; Mitral Regurgitation
MAUDE report 6692855 ↗
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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