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AMS 700 72403900Recalls & reported problems

American Medical Systems, Inc. · Tactile Pump with InhibiZone · Class 3 · Implant

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 00878953002439), received between Oct 14, 2021 and Oct 14, 2021 — 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

  • Unspecified Infection1

Recent adverse event reports

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

  • InjuryOct 14, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE PATIENT EXPERIENCED INFECTION WITH THIS INFLATABLE PENILE PROSTHESIS (IPP). THE ENTIRE DEVICE WAS REMOVED AND REPLACED WITH A TACTRA MALLEABLE PROSTHESIS. NO ADDITIONAL PATIENT COMPLICATIONS WERE REPORTED.

    Patient problems: Unspecified Infection

    MAUDE report 12635794 ↗

Other Prosthesis, Penis, Inflatable devices

All Prosthesis, Penis, Inflatable devices →

Sources and updates

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