ANTHOLOGY 71357108Recalls & reported problems
Smith & Nephew, Inc. · ANTHOLOGY HIGH OFFSET POROUS PLUS HYDROXYAPATITE SIZE 8 · Class 2 · Implant
All models of ANTHOLOGY (69)
Data updated Oct 18, 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 03596010559630), received between Feb 20, 2018 and Aug 11, 2020 — classified as 4 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 18, 2026.
Most reported problems
Device problems
- Insufficient Device Problem Information2
- Adverse Event Without Identified Device or Use Problem1
- Fracture1
Patient problems
- Injury3
- Failure of Implant1
- No Information1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryAug 11, 2020Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED THAT, AFTER A THR HAD BEEN PERFORMED, THE PATIENT EXPERIENCED AN UNIDENTIFIED ADVERSE EVENT. A REVISIONS SURGERY WAS PERFORMED TO EXCHANGE THE ANTHOLOGY HIGH OFFSET POROUS PLUS HA STEM SIZE 8. THE PATIENT OUTCOME IS UNKNOWN.
Patient problems: Injury; No Information
MAUDE report 10394404 ↗InjuryMay 22, 2019Fracture; Fracture
IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED DUE TO A FRACTURED STEM.
Patient problems: Injury
MAUDE report 8634421 ↗InjuryApr 4, 2018Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED DUE TO A LOOSE STEM. STEM AND FEMORAL HEAD WERE REMOVED.
Patient problems: Injury
MAUDE report 7397064 ↗InjuryFeb 20, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED BECAUSE THE IMPLANT HAVE SUBSIDED.
Patient problems: Failure of Implant
MAUDE report 7283979 ↗
Other Prosthesis, hip, semi-constrained, metal/polymer, cemented devices
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- 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
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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