Accolade 6721-1040Recalls & 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
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 04546540669551), received between Jun 29, 2020 and Apr 1, 2024 — classified as 3 injuries.
The most frequently reported specific device problem is “Corroded” (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.
Reports received per month
Most reported problems
Device problems
- Corroded1
- Insufficient Device Problem Information1
- Material Erosion1
- Unstable1
Patient problems
- Bone Fracture(s)1
- Injury1
- Joint Laxity1
- Metal Related Pathology1
- Pain1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryApr 1, 2024Unstable; Unstable
PATIENT REVISED DUE TO INSTABILITY. THIS IS THE RIGHT SIDE. DR. THOUGHT THE PATIENT WAS IMPINGING POSTERIORLY SO WE PUT IN A NEUTRAL LINER. WE WASTED A LINER AS IT STILL FELT UNSTABLE, AND WE IMPLANTED THE 0° ECCENTRIC LINER LISTED ON THE SHEET. NO OTHER INFORMATION AVAILABLE DUE TO HOSPITAL POLICY.
Patient problems: Joint Laxity
MAUDE report 19015533 ↗InjuryOct 6, 2023Corroded; Material Erosion; Corroded; Material Erosion
LEFT HIP REVISION FOR PAIN AND ELEVATED COBALT LEVELS. COCR HEAD REPLACED WITH A UNIVERSAL TAPER SLEEVE AND CERAMIC HEAD, INSERT EXCHANGED TO AN ECCENTRIC.
Patient problems: Metal Related Pathology; Pain
MAUDE report 17883685 ↗InjuryJun 29, 2020Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED THAT THE PATIENT'S LEFT HIP WAS REVISED DUE TO A FEMORAL PERIPROSTHETIC FRACTURE LEADING TO STEM SUBSIDENCE. AN ACCOLADE II STEM, BIOLOX HEAD, AND 36F LINER WERE REVISED TO ANOTHER 36F LINER AND COMPETITOR HEAD AND STEM. REP CONFIRMED THERE ARE NO ALLEGATIONS AGAINST THE REVISED HEAD AND LINER, AND THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.
Patient problems: Bone Fracture(s); Injury
MAUDE report 10205476 ↗
Other PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED devices
- PINNACLE 1217-25-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED735 reports
- NA 1365-52-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED683 reports
- APEX 1246-03-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED3 deaths613 reports
- PINNACLE 1217-20-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 deaths590 reports
- PINNACLE 1217-30-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 death484 reports
- NA 1365-53-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED404 reports
- PINNACLE ALTRX 1221-36-054Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED388 reports
- PINNACLE ALTRX 1221-32-050Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED386 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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