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MENTOR MemoryGel BOOST Breast Implant SMPB130Recalls & reported problems

Mentor Texas L.P. · Smooth Moderate Plus Profile, 130cc |Smooth|Round|Silicone| · Class 3 · Implant

All models of MENTOR MemoryGel Breast Implants (368) · MENTOR MemoryGel BOOST Breast Implant (53)

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

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00081317026792), received between Dec 8, 2022 and Dec 8, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Deformation” (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 Deformation1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionDec 8, 2022Material Deformation; Material Deformation

    IT WAS REPORTED THAT A 130CC MENTOR MEMORYGEL BOOST BREAST IMPLANT IN WAS FOUND TO BE DEFORMED OUT OF THE BOX. NO ADVERSE EVENT WAS EXPERIENCED BY ANY PATIENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15945994 ↗

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

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

Sources and updates

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