Avenir Complete™ 574203030Recalls & reported problems
Zimmer, Inc. · Class 2 · Implant
All models of Avenir Complete (37)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024509283), received between Jan 2, 2026 and Jan 26, 2026 — classified as 2 injuries.
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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
Patient problems
- Bone Fracture(s)1
- Periprosthetic fracture1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJan 26, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT APPROXIMATELY THREE WEEKS POST-IMPLANTATION, THE PATIENT UNDERWENT A HIP REVISION DUE TO PERIPROSTHETIC FEMUR FRACTURE. THE FRACTURE OCCURRED WHILE THE PATIENT WAS CHANGING THEIR CLOTHES AND FELL, POSSIBLY DUE TO LOSING THEIR BALANCE WHILE ON ONE FOOT. THE STEM WAS REVISED AND THE FRACTURE FIXED WITH A CABLE. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Periprosthetic fracture
MAUDE report 24178192 ↗InjuryJan 2, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT FOLLOWING A PRIMARY TOTAL HIP REPLACEMENT, THE PATIENT REQUIRED STEM REVISION APPROXIMATELY 4 DAYS POST-IMPLANTATION DUE TO A LESSER TROCHANTER FRACTURE IDENTIFIED AFTER ONSET OF PAIN UPON STANDING. APPROXIMATELY 1 DAY POST-IMPLANTATION, THE PATIENT STOOD AND EXPERIENCED PAIN; IMAGING DEMONSTRATED A LESSER TROCHANTER FRACTURE, WITH NO FALL REPORTED. SUBSEQUENTLY, THE STEM WAS REVISED TO A REVISION TOTAL HIP REPLACEMENT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Bone Fracture(s)
MAUDE report 23942792 ↗
Other Prosthesis, hip, semi-constrained, metal/polymer, uncemented devices
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- Endo-Model SL Knee Prosthesis System 16-2840/02WALDEMAR LINK GmbH & Co. KG · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented1 recall17 reports
- Endo-Model SL Knee Prosthesis System 16-2840/05WALDEMAR LINK GmbH & Co. KG · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented1 recall12 reports
- Trident 623-10-36EHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, uncemented57 reports
- LFIT 6260-9-336Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, uncemented56 reports
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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