Avenir® Müller 01.06010.305Recalls & reported problems
Zimmer GmbH · Class 2 · Implant
Data updated Oct 16, 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 00889024590823), received between Aug 3, 2021 and Aug 3, 2021 — classified as 1 malfunction.
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Insufficient Device Problem Information1
- Loosening of Implant Not Related to Bone-Ingrowth1
Patient problems
- Extraskeletal ossification1
- Inadequate Osseointegration1
- Insufficient Information1
- Osteolysis1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 3, 2021Insufficient Device Problem Information; Loosening of Implant Not Related to Bone-Ingrowth; Insufficient Device Problem Information; Loosening of Implant Not Related to Bone-Ingrowth
THIS FOLLOW-UP IS BEING SUBMITTED BECAUSE THE DEVICE REPORTED IN THIS MEDWATCH WAS NOT REVISED BUT IMPLANTED DURING THE REVISION SURGERY. THERE IS NO ADVERSE EVENT REPORTED AFTER THE IMPLANTATION OF THIS DEVICE THEREFORE THIS COMPLAINT WILL BE INVALIDATED PLEASE DELETE IT FROM YOUR RECORDS.
Patient problems: Extraskeletal ossification; Inadequate Osseointegration; Insufficient Information; Osteolysis
MAUDE report 12265735 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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