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NATRELLE INSPIRA Single Use Sizers SSZ-F415Recalls & reported problems

Allergan, Inc. · Natrelle Inspira FullProf 415cc SSZ US · Class U

All models of Natrelle Breast Implants (1167) · NATRELLE INSPIRA Single Use Sizers (16)

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 10888628045095), received between Jan 25, 2023 and Jan 25, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Handling Problem” (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

  • Device Handling Problem1

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.

  • MalfunctionJan 25, 2023Device Handling Problem; Device Handling Problem

    HEALTHCARE PROFESSIONAL REPORTED "THAT THE INNER THERMOFORM AND OUTER THERMOFORM TRAYS WERE STUCK TOGETHER ON ALL THE SIZERS THAT WERE USED FOR THE CASE. WE WERE STILL ABLE TO USE THE SIZERS, BUT POSES A GREAT CONCERN TO STERILITY." DEVICE HAS NOT BEEN IMPLANTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16241439 ↗

Other Sizer, Mammary, Breast Implant Volume devices

All Sizer, Mammary, Breast Implant Volume devices →

Sources and updates

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