Accolade 6021-0740Recalls & 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 04546540510723), received between Jan 23, 2019 and Jun 14, 2023 — classified as 3 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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.
Most reported problems
Device problems
- Insufficient Device Problem Information2
- Detachment of Device or Device Component1
Patient problems
- Injury2
- Pain2
- Reaction2
- Inflammation1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryJun 14, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT THE PATIENT'S LEFT HIP WAS REVISED. AS REPORTED: "PATIENT INITIALLY PRESENTED TO CLINIC WHERE HE COMPLAINED OF PAIN IN HIS LEFT HIP. X-RAY REVEALED CATASTROPHIC FAILURE OF FEMORAL HEAD WITH FEMORAL HEAD DISSOCIATION. DAMAGE TO STEM AND CUP NECESSITATED REVISION OF ALL COMPONENTS. ALL COMPONENTS WERE WELL FIXED BUT EXPLANTED DUE TO DAMAGE. EXPLANTS WERE NOT AVAILABLE FOR RETURN."
Patient problems: Pain
MAUDE report 17124024 ↗InjuryOct 22, 2019Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED BY PATIENT'S ATTORNEY AS A RESULT OF A LEGAL CLAIM THAT ALLEGEDLY ON (B)(6) 2012 THE PATIENT WAS IMPLANTED WITH A STRYKER V40 FEMORAL HEAD ON HIS RIGHT HIP. IT IS FURTHER ALLEGED "SUBSEQUENTLY HE DEVELOPED PROGRESSIVE GROIN PAIN AND RIGHT HIP PAIN AND A COBALT ION LEVEL THAT WAS EXTREMELY HIGH. DUE TO THIS, REVISION WAS PERFORMED ON (B)(6) 2019."
Patient problems: Inflammation; Injury; Pain; Reaction
MAUDE report 9221084 ↗InjuryJan 23, 2019Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED BY THE ATTORNEY THAT PLAINTIFF UNDERWENT A TOTAL HIP ARTHROPLASTY ON (B)(6) 2010 AND HAD TO UNDERGO REVISION SURGERY ON (B)(6) 2017 DUE TO ALLEGED ALTR.
Patient problems: Injury; Reaction
MAUDE report 8272518 ↗
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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