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Alloclassic® Zweymüller® HipStem 2840Recalls & reported problems

Zimmer GmbH · Class 2 · Implant

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 00889024481084), received between Dec 5, 2019 and Dec 5, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Insufficient Device Problem Information1

Patient problems

  • Wound Dehiscence1

Recent adverse event reports

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

  • InjuryDec 5, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

    PATIENT WAS IMPLANTED ON THE RIGHT SIDE AND IT WAS REPORTED THAT POST SURGERY THE WOUND SHOWED REPEATED SYMPTOMS OF REDNESS, SWELLING, RUPTURE AND EXUDATION. THEREFORE THE PATIENT UNDERWENT A DILATED AND INVASIVE CATHETER DRAINAGE, AND THE WOUND HEALED UPON DISCHARGE.

    Patient problems: Wound Dehiscence

    MAUDE report 9415107 ↗

Other Prosthesis, hip, hemi-, femoral, metal devices

All Prosthesis, hip, hemi-, femoral, metal devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.