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MENTOR MemoryGel Breast Implant 3545240Recalls & reported problems

Mentor Texas L.P. · SILTEX Round Ultra High Profile Silicone Gel-Filled Breast Implant, 240cc |Textured|Round|Silicone| · Class 3 · Implant

All models of MENTOR MemoryGel Breast Implants (368) · MENTOR MemoryGel Breast Implant (211)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00081317007081), received between Jun 8, 2021 and Jun 8, 2021 — classified as 1 injury.

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 Problem1

Patient problems

  • Capsular Contracture1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJun 8, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT A (B)(6) YEAR OLD FEMALE PATIENT, WHO'S UNDERGONE BREAST AUGMENTATION REVISION WITH A 240CC MENTOR MEMORYGEL BREAST IMPLANT ON THE LEFT BREAST, SUFFERED LEFT BREAST CAPSULAR CONTRACTURE (BAKER GRADE III), POST-PROCEDURE. THE CAPSULAR CONTRACTURE WAS DIAGNOSED DURING AN IN-OFFICE VISIT. AT THE TIME OF THIS REPORT, MENTOR HAS RECEIVED NO INFORMATION REGARDING EXPLANTATION OR AN EXPECTED EXPLANTATION DATE.

    Patient problems: Capsular Contracture

    MAUDE report 11963325 ↗

Other Prosthesis, breast, noninflatable, internal, silicone gel-filled devices

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Sources and updates

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