Avenir Complete™ 574102060Recalls & reported problems
Zimmer, Inc. · Class 2 · Implant
All models of Avenir Complete (37)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00889024508798), received between Apr 19, 2022 and Dec 15, 2023 — classified as 4 injuries.
The most frequently reported specific device problem is “Fracture” (2 reports).
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.
Reports received per month
Most reported problems
Device problems
- Fracture2
- Migration2
Patient problems
- Bone Fracture(s)2
- Implant Pain2
- Necrosis2
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryDec 15, 2023Migration; Migration
IT WAS REPORTED THE PATIENT WAS DIAGNOSED WITH PERI PROSTHETIC FRACTURE. THE PATIENT WAS HAVING MORE THAN NORMAL PAIN AT REHABILITATION. THERE WAS NO TRAUMA OR SUDDEN PAIN REPORTED. PATIENT HAD A CT SCAN THAT REVEALED A FEMORAL FISSURATION WITH A 2-3MM SUBSIDENCE OF THE STEM COMPARED TO THE DIRECT POST OP RADIOGRAPH. A CERCLAGE OF THE FEMUR WAS PERFORMED, AND ALL IMPLANTS MAINTAINED IMPLANTED.
Patient problems: Bone Fracture(s); Implant Pain
MAUDE report 18334468 ↗InjuryOct 5, 2023Migration; Migration
NO ADDITIONAL EVENT INFORMATION TO REPORT AT TIS TIME.
Patient problems: Bone Fracture(s); Implant Pain
MAUDE report 17878505 ↗InjuryApr 14, 2023Fracture; Fracture
IT WAS REPORTED PATIENT UNDERWENT INITIAL HIP ARTHROPLASTY. SUBSEQUENTLY THE PATIENT EXPERIENCED NECROSIS AND LOSS OF ACTIVITY APPROXIMATELY ONE YEAR POST IMPLANTATION. REVIEW OF CT SCAN SHOWS POSSIBLE IMPLANT FRACTURE. NO REVISION HAS BEEN REPORTED TO DATE. THERE IS NO ADDITIONAL INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Necrosis
MAUDE report 16744221 ↗InjuryApr 19, 2022Fracture; Fracture
IT WAS REPORTED PATIENT UNDERWENT INITIAL HIP ARTHROPLASTY. SUBSEQUENTLY THE PATIENT EXPERIENCED NECROSIS AND LOSS OF ACTIVITY APPROXIMATELY ONE YEAR POST IMPLANTATION. REVIEW OF CT SCAN SHOWS POSSIBLE IMPLANT FRACTURE. NO REVISION HAS BEEN REPORTED TO DATE. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.
Patient problems: Necrosis
MAUDE report 14141006 ↗
Other Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented devices
- STAGEONE 431209Biomet Orthopedics, LLC · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented2 recalls0 reports
- SELF CENTERING 1035-45-000Depuy Orthopaedics, Inc. · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented84 reports
- LFIT 6260-9-036Howmedica Osteonics Corp. · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented80 reports
- ACTIS 101011060Depuy (Ireland) · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented66 reports
- RINGLOC BI-POLAR HIP SYSTEM 11-165228Biomet Orthopedics, LLC · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 recall1 death12 reports
- SELF CENTERING 1035-44-000Depuy Orthopaedics, Inc. · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented60 reports
- TANDEM 71324046Smith & Nephew, Inc. · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 recall9 reports
- TAPERLOC COMPLETE XR 123 MICRO FEMORAL 51-145170Biomet Orthopedics, LLC · Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented59 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page