Alumina 17-3200ERecalls & reported problems
Howmedica Osteonics Corp. · Alumina Ceramic C-Taper Femoral Head · Class 2 · Implant
All models of Alumina (16)
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 07613327101249), received between Aug 8, 2018 and Apr 5, 2022 — classified as 4 injuries.
The most frequently reported specific device problem is “Degraded” (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
- Degraded1
- Device Dislodged or Dislocated1
- Insufficient Device Problem Information1
- Noise, Audible1
- Scratched Material1
Patient problems
- Pain4
- Injury3
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryApr 5, 2022Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED THAT THE PATIENT'S LEFT HIP WAS REVISED DUE TO PAIN IN FLEXION AND AUDIBLE CLICKING. A CERAMIC HEAD, INSERT AND METAL SLEEVE WERE REVISED TO A CERAMIC HEAD WITH POLY INSERT. REP CONFIRMED THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.
Patient problems: Pain
MAUDE report 14009758 ↗InjuryJul 18, 2019Degraded; Device Dislodged or Dislocated; Degraded; Device Dislodged or Dislocated
FRACTURED AND WORN CERAMIC LINER. WORN CERAMIC HEAD. REPLACED LINER AND HEAD AND SLEEVE. REPLACEMENT WAS A X3 POLY LINER AND CERAMIC HEAD AFTER IN-DEPTH DISCUSSION REGARDING BEARING SURFACES AND POSSIBILITY OF CERAMIC FRAGMENTS CAUSING THIRD BODY WEAR OF A POLY LINER. WAS CLIMBING LADDER TO ACCESS TREE APPROX 2/12 PRIOR TO REVISION SURGERY. ONLY NOTICED INCREASE IN PAIN, HENCE PRESENTING 2 MONTHS POST EVENT.
Patient problems: Injury; Pain
MAUDE report 8804644 ↗InjuryNov 2, 2018Scratched Material; Scratched Material
THE CUSTOMER REPORTED THAT THE PATIENT PRESENTED WITH PAIN AND X-RAY CONFIRMED THAT HIS EXETER STEM HAD FRACTURED AT THE NECK, REQUIRING REVISION. MAR CONFIRMS WEAR OF THE CERAMIC HEAD.
Patient problems: Injury; Pain
MAUDE report 8032481 ↗InjuryAug 8, 2018Noise, Audible; Noise, Audible
IT WAS REPORTED THAT PATIENT'S RIGHT HIP WAS REVISED DUE TO PAIN AND AUDIBLE NOISE. PATIENT WAS REVISED FROM A CERAMIC HEAD AND LINER TO A 36 +5 CERAMIC HEAD WITH 36E POLY LINER.
Patient problems: Injury; Pain
MAUDE report 7763589 ↗
Other Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented devices
- BIOLOX DELTA 1365-32-310Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented551 reports
- PINNACLE ALTRX 1221-36-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented481 reports
- BIOLOX DELTA 1365-32-320Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 death314 reports
- BIOLOX DELTA 1365-36-720Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 death189 reports
- DJO SURGICAL 400-03-362Encore Medical, L.P. · Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented187 reports
- Anthology 71365705Smith & Nephew, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented176 reports
- BIOLOX DELTA 1365-40-710Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented170 reports
- PINNACLE GRIPTION 1217-32-054Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented169 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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