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Natrelle INSPIRA Breast Implants SRL-125Recalls & reported problems

Allergan, Inc. · NATRELLE INSPIRA Sty SRL-125 Low profile |smooth|round|silicone · Class 3 · Implant

All models of Natrelle Breast Implants (1167) · Natrelle INSPIRA Breast Implants (197)

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

Adverse event reports
9
Deaths reported
0
Injuries reported
9
Recalls naming it
0

Summary

The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 10888628006652), received between Jul 10, 2020 and Sep 22, 2026 — classified as 9 injuries.

The most frequently reported specific device problem is “Device Appears to Trigger Rejection” (7 reports).

4 other recalls cover devices cleared under the same FDA submission (P020056); they may or may not involve this specific model.

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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 2 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 1 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Device Appears to Trigger Rejection7
  • Material Rupture1
  • Patient-Device Incompatibility1

Patient problems

  • Capsular Contracture8
  • Failure of Implant1

Recent adverse event reports

The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.

  • InjurySep 22, 2026Device Appears to Trigger Rejection

    Healthcare professional reported "Capsular Contracture Baker Grade III". This record is for the left side. Device remains implanted.

    Patient problems: Capsular Contracture

    MAUDE report 50859773 ↗
  • InjuryApr 29, 2025Device Appears to Trigger Rejection; Device Appears to Trigger Rejection

    HEALTHCARE PROFESSIONAL REPORTED "CAPSULAR CONTRACTURE BAKER GRADE III, WRINKLING/RIPPLING, CORRECTION OF ASYMMETRY". THIS RECORD IS FOR THE LEFT SIDE. DEVICE HAS BEEN EXPLANTED AND REPLACED.

    Patient problems: Capsular Contracture

    MAUDE report 21929494 ↗
  • InjuryApr 23, 2025Device Appears to Trigger Rejection; Device Appears to Trigger Rejection

    HEALTHCARE PROFESSIONAL REPORTED "CAPSULAR CONTRACTURE BAKER GRADE III, DEVICE MIGRATION/IMPLANT MALPOSITION, WRINKLING/RIPPLING". THIS RECORD IS FOR THE RIGHT SIDE. DEVICE HAS BEEN EXPLANTED AND REPLACED.

    Patient problems: Capsular Contracture

    MAUDE report 21896051 ↗
  • InjuryApr 14, 2023Device Appears to Trigger Rejection; Device Appears to Trigger Rejection

    HEALTHCARE PROFESSIONAL REPORTED THE EVENT OF RIGHT SIDE CAPSULAR CONTRACTURE BAKER GRADE III. DEVICE REMAINS IMPLANTED.

    Patient problems: Capsular Contracture

    MAUDE report 16743260 ↗
  • InjuryApr 18, 2022Device Appears to Trigger Rejection; Device Appears to Trigger Rejection

    HEALTHCARE PROFESSIONAL REPORTED "CAPSULAR CONTRACTURE, BAKER GRADE IV" AGAINST LEFT DEVICE. THE DEVICE HAS BEEN EXPLANTED.

    Patient problems: Capsular Contracture

    MAUDE report 14135440 ↗
  • InjuryNov 2, 2021Material Rupture; Material Rupture

    DEVICE HAS BEEN EXPLANTED.

    Patient problems: Failure of Implant

    MAUDE report 12741224 ↗
  • InjuryJul 15, 2021Device Appears to Trigger Rejection; Device Appears to Trigger Rejection

    HEALTHCARE PROFESSIONAL REPORTED LEFT SIDE CAPSULAR CONTRACTURE, BAKER GRADE IV. DEVICE HAS BEEN EXPLANTED.

    Patient problems: Capsular Contracture

    MAUDE report 12175782 ↗
  • InjuryJul 15, 2021Device Appears to Trigger Rejection; Device Appears to Trigger Rejection

    DEVICE HAS BEEN REPLACED.

    Patient problems: Capsular Contracture

    MAUDE report 12174604 ↗
  • InjuryJul 10, 2020Patient-Device Incompatibility; Patient-Device Incompatibility

    HEALTHCARE PROFESSIONAL NOTED LEFT SIDE CAPSULAR CONTRACTURE BAKER GRADE III/IV AND PAIN DUE TO TIGHTNESS OF THE BREASTS.

    Patient problems: Capsular Contracture

    MAUDE report 10258727 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under P020056. One submission often covers many models, so check the product and lot details in each record.

  • Z-0701-2020 · Nov 6, 2019 · Terminated
    Natrelle Inspira Sillicone-Filled Breast Implants for the following Styles and Sizes: 7607 SSM, 7608 SSF, 7609 SSX, 7513 SRL, 7514 SRLP, 7515 SRM, 7516 SRF, 7517 SRX, 7626 SCL, 762
  • Z-0700-2020 · Nov 6, 2019 · Terminated
    Natrelle Silicone Filled Breast Implants for the following Styles and Sizes: Style 10, Style 15, Style 20, Style 40, Style 45 Style 10/UDI: NATRELLE Style 10-180 Gel Round Mod
  • Z-2454-2019 · Jul 24, 2019 · Open, Classified
    Natrelle and McGhan Silicone-Filled Breast Implant BioCell Round Moderate Profile, Sterile, for the following style numbers: Style 110:110-090, 110-120, 110-150, 110-180, 110-
  • Z-2453-2019 · Jul 24, 2019 · Open, Classified
    Natrelle Inspira, Silicone-Filled Breast Implants, Sterile, for the following style numbers: Style TRL: TRL-110TRL-125,TRL-140,TRL-170,TRL-200,TRL-230,TRL-260,TRL-290,TRL-320,TR

Other Prosthesis, Breast, Noninflatable, Internal, Silicone Gel-Filled devices

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Sources and updates

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