Skip to content

MENTOR MemoryGel Breast Implant 3541007Recalls & reported problems

Mentor Texas L.P. · SILTEX Round Moderate Profile Gel-Filled Breast Implant, 100cc · 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 00081317000594), received between Nov 1, 2019 and Nov 1, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Material Rupture” (1 report).

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

  • Material Rupture1

Patient problems

  • Pain1
  • Skin Irritation1

Recent adverse event reports

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

  • InjuryNov 1, 2019Material Rupture; Material Rupture

    IT WAS REPORTED THAT A FEMALE PATIENT WITH UNKNOWN AGE AND RACE UNDERWENT UNSPECIFIED BREAST RECONSTRUCTION SURGERY WITH 100CC MENTOR MEMORYGEL BREAST IMPLANT AND WAS PRESENTED WITH RIGHT SIDE RUPTURE, ACUTE DERMATITIS, AND LOWER BACK PAIN. AT THE TIME OF THIS REPORT, MENTOR HAS RECEIVED NO INFORMATION REGARDING EXPLANTATION OR AN EXPECTED EXPLANTATION DATE.

    Patient problems: Pain; Skin Irritation

    MAUDE report 9268885 ↗

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

All Prosthesis, breast, noninflatable, internal, silicone gel-filled devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page