ANTHOLOGY 71357109Recalls & reported problems
Smith & Nephew, Inc. · ANTHOLOGY HIGH OFFSET POROUS PLUS HYDROXYAPATITE SIZE 9 · Class 2 · Implant
All models of ANTHOLOGY (69)
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 03596010559647), received between Aug 7, 2019 and Apr 19, 2023 — classified as 3 injuries.
The most frequently reported specific device problem is “Fracture” (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
- Adverse Event Without Identified Device or Use Problem1
- Fracture1
- Insufficient Device Problem Information1
Patient problems
- Bone Fracture(s)2
- Failure of Implant1
- Fall1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryApr 19, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT, APPROXIMATELY ONE WEEK AFTER A THR SURGERY, WHERE AN OXINIUM FEM HD 12/14 36 MM +0 AND AN ANTHOLOGY HO POR PL HA SZ 9 WERE IMPLANTED, THE PATIENT TWISTED THEIR LEG, AND FELT A CRACK. THE PATIENT THEN PRESENTED TO THE HOSPITAL WHERE AN X-RAY REVEALED A PERI-PROSTHETIC FRACTURE, SO A REVISION SURGERY WAS DONE, AND A REDAPT STEM WAS IMPLANTED. NO OTHER COMPLICATIONS WERE REPORTED.
Patient problems: Bone Fracture(s)
MAUDE report 16772432 ↗InjurySep 29, 2021Fracture; Fracture
IT WAS REPORTED THAT, AFTER TOTAL HIP REPLACEMENT WAS PERFORMED ON AN UNSPECIFIED DATE, THE PATIENT SUSTAINED A PERIPROSTHETIC FRACTURE FOLLOWING A FALL. THIS ADVERSE EVENT WAS TREATED WITH A REVISION SURGERY CONDUCTED ON (B)(6) 2021. PATIENT'S CURRENT HEALTH STATUS IS UNKNOWN.
Patient problems: Failure of Implant; Fall
MAUDE report 12550868 ↗InjuryAug 7, 2019Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED THAT THE PATIENT HAD A FEMORAL FRACTURE REQUIRING WIRING TREATMENT. THE PATIENT RECOVERED FROM THE ADVERSE EVENT AND WAS DISCHARGED THE (B)(6) 2019.
Patient problems: Bone Fracture(s)
MAUDE report 8867909 ↗
Other Prosthesis, hip, semi-constrained, metal/polymer, cemented devices
- NA 1365-51-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented753 reports
- NA 1365-50-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented412 reports
- ARTICUL/EZE 1365-21-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall280 reports
- ARTICUL/EZE 1365-11-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 death262 reports
- LFIT 6260-9-236Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, cemented256 reports
- PINNACLE GRIPTION 1217-32-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented2 deaths239 reports
- ELEOS™ 25002111EOnkos Surgical, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented3 deaths230 reports
- Novation 130-36-52Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented2 recalls124 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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