Accolade 6077-0230Recalls & reported problems
Howmedica Osteonics Corp. · 127 Degree Neck Angle Hip Stem · Class 2 · Implant
All models of Accolade (57)
Data updated Oct 16, 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 07613327021189), received between Aug 28, 2018 and Aug 28, 2018 — classified as 1 injury.
The most frequently reported specific device problem is “Loss of Osseointegration” (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
- Loss of Osseointegration1
- Migration1
Patient problems
- Inadequate Osseointegration1
- Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 28, 2018Loss of Osseointegration; Migration; Loss of Osseointegration; Migration
IT WAS REPORTED BY PATIENT'S ATTORNEY THAT THE PATIENT WAS IMPLANTED WITH A STRYKER HIP SYSTEM AND UNDERWENT REVISION SURGERY. UPDATE: ON (B)(6) 2017 A RIGHT HIP HEMIARTHROPLASTY REVISION AND REMOVAL OF FEMORAL HEAD AND REIMPLANTATION OF A BIPOLAR HIP ARTHROPLASTY WAS PERFORMED FOR A PRE-OPERATIVE DIAGNOSIS OF "FAILED RIGHT HIP HEMIARTHROPLASTY ... WITH RIGHT HIP DISASSOCIATION FROM UNITRAX HEAD COMPONENT ... AND POSSIBLE LOOSENING. IN THIS (B)(6) PATIENT, FAILURE TO GAIN BIOLOGIC FIXATION WITH EARLY POSTOPERATIVE EVIDENCE OF STEM SUBSIDENCE PROGRESSED TO FURTHER SUBSIDENCE RESULTING IN IMPINGEMENT OF THE HOST FEMORAL NECK AND THE UNITRAX HEAD, WHICH ULTIMATELY RESULTED IN DISASSOCIATING IT FROM THE TRUNNION.
Patient problems: Inadequate Osseointegration; Injury
MAUDE report 7823064 ↗
Other Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous devices
- Accolade 6021-0537Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous46 reports
- PROFEMUR® PHAC1252Microport Orthopedics Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous37 reports
- Accolade 6020-0335Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous35 reports
- OXINIUM 71342340Smith & Nephew, Inc. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous32 reports
- EXETER 0580-1-351Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous29 reports
- INSTRUMENT 2101-0200Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous27 reports
- REFLECTION 71330001Smith & Nephew, Inc. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous20 reports
- Accolade 6720-0330Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous18 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.
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