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Wagner SL Revision® 01.00109.119Recalls & reported problems

Zimmer GmbH · Class 2

All models of Wagner SL Revision (33)

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 00889024277854), received between May 18, 2022 and May 18, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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

  • Fracture1

Patient problems

  • Failure of Implant1

Recent adverse event reports

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

  • InjuryMay 18, 2022Fracture; Fracture

    IT WAS REPORTED THAT DURING SURGERY THE LOCKING SCREW OF THE TRIAL STEM BROKE LEAVING THE DISTAL SEGMENT OF THE STEM IN THE FEMUR. AN EXTENDED TROCHANTERIC OSTEOTOMY HAD TO BE PERFORMED TO EXTRACT THE DISTAL SEGMENT OF THE STEM. SURGERY WAS EXTENDED BY BETWEEN AN HOUR TO 90 MINUTES DUE TO THE OSTEOTOMY. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

    Patient problems: Failure of Implant

    MAUDE report 14433039 ↗

Other Prosthesis, hip, semi-constrained, metal/polymer, cemented devices

All Prosthesis, hip, semi-constrained, metal/polymer, cemented devices →

Sources and updates

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