Centrax 6226-2-642Recalls & reported problems
Howmedica Osteonics Corp. · Bipolar Duration Stabilized · Class 2 · Implant
All models of Centrax (12)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613327032154), received between Feb 22, 2018 and May 6, 2021 — classified as 2 injuries, 1 malfunction.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 18, 2026.
Most reported problems
Device problems
- Device Dislodged or Dislocated1
- Insufficient Device Problem Information1
- Mechanical Problem1
Patient problems
- Injury1
- Insufficient Information1
- Joint Dislocation1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryMay 6, 2021Insufficient Device Problem Information; Insufficient Device Problem Information
NEUROVASCULAR DISORDER ON (B)(6) 2018. TREATED WITH ORTOP. UPDATE APRIL 29, 2021: THIS EVENT WAS REPORTED AS MULTICENTER RESULTS SURVEY AT BHA AND PROVIDED BY CLINICAL. ACCORDING TO SURGEON, NEUROVASCULAR DISORDER IS RELATED TO PROCEDURE. BUT IT IS UNKNOWN IF IT IS RELATED TO DEVICE OR ONLY PROCEDURE. IT CAN BE ¿CAUSAL RELATIONSHIP¿ IS UNKNOWN, TOO.
Patient problems: Insufficient Information
MAUDE report 11784817 ↗MalfunctionJun 18, 2019Mechanical Problem; Mechanical Problem
IT WAS REPORTED THAT, A SURGEON NOTICED A GAP (2MM) BETWEEN LOCKING RING AND SHELL. A SPARE CENTRAX WAS IMPLANTED INSTEAD. UPDATE: "THERE WAS A GAP (2MM) BETWEEN THE LOCKING RING AND ACETABULAR SHELL."
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8707625 ↗InjuryFeb 22, 2018Device Dislodged or Dislocated; Device Dislodged or Dislocated
ARTIFICIAL FEMORAL HEAD HAD A POSTERIOR DISLOCATION (B)(6). HEAD WAS REDUCED, BUT IT DISLOCATED AGAIN.
Patient problems: Injury; Joint Dislocation
MAUDE report 7289992 ↗
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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