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AGILITY 1555-33-020Recalls & reported problems

Depuy Orthopaedics, Inc. · AGILITY TOTAL ANKLE SYSTEM ANKLE INSERT SIZE 3 +2 · Class 2 · 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 10603295058717), received between Oct 23, 2018 and Oct 23, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Naturally Worn” (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

  • Naturally Worn1

Patient problems

  • Loss of Range of Motion1
  • No Code Available1

Recent adverse event reports

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

  • InjuryOct 23, 2018Naturally Worn; Naturally Worn

    IT WAS REPORTED THAT THE PATIENT HAD REDUCED RANGE OF MOTION. THE INSERT WAS REVISED/EXCHANGED. LIMITED POLY WEAR.

    Patient problems: Loss of Range of Motion; No Code Available

    MAUDE report 7996020 ↗

Other PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER devices

All PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER devices →

Sources and updates

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