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MENTOR MemoryGel Xtra Breast Implant THPX175Recalls & reported problems

Mentor Texas L.P. · SILTEX High Profile Xtra Silicone Gel-Filled Breast Implant, 175cc |Textured|Round|Silicone| · Class 3 · Implant

All models of MENTOR MemoryGel Breast Implants (368) · MENTOR MemoryGel Xtra Breast Implant (88)

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 00081317025627), received between Oct 18, 2022 and Oct 18, 2022 — 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.

  • InjuryOct 18, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT A FEMALE PATIENT UNDERWENT A BREAST AUGMENTATION WITH A 125CC MENTOR MEMORYGEL BREAST IMPLANT (LEFT) AND A 175CC MENTOR MEMORYGEL XTRA BREAST IMPLANT (RIGHT) AND EXPERIENCED BILATERAL CAPSULAR CONTRACTURE, BAKER GRADE 3 POST-OPERATIVELY. AS A RESULT, THE PATIENT UNDERWENT EXPLANTATION ON (B)(6) 2022. THIS REPORT IS FOR THE RIGHT SIDE DEVICE.

    Patient problems: Capsular Contracture

    MAUDE report 15628813 ↗

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

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Sources and updates

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