Alumina 17-32-3ERecalls & reported problems
Howmedica Osteonics Corp. · 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
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04546540195616), received between Sep 10, 2018 and Jun 6, 2019 — classified as 2 injuries.
The most frequently reported specific device problem is “Noise, Audible” (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
- Noise, Audible2
Patient problems
- Injury2
- Discomfort1
- Irritation1
- Pain1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJun 6, 2019Noise, Audible; Noise, Audible
IT WAS REPORTED THAT THE PATIENTS LEFT HIP WAS REVISED AFTER PATIENT COMPLAINT OF SQUEAKING EVENTUALLY PATIENT COMPLAINT OF A GRINDING NOISE. INTRA-OP AND POST-OP INSPECTIONS FOUND NO FRACTURES, WEAR, OR DAMAGE TO THE CERAMIC HEAD AND LINER. NO CERAMIC DEBRIS WAS NOTED IN THE PATIENT. PATIENT WAS REVISED TO A POLY LINER WITH A CERAMIC HEAD AND SLEEVE.
Patient problems: Injury
MAUDE report 8675664 ↗InjurySep 10, 2018Noise, Audible; Noise, Audible
IT WAS REPORTED THAT, "IT WAS REPORTED AS A RESULT OF A FILED LAWSUIT; ON OR ABOUT (B)(6) 2006, THE PATIENT UNDERWENT A TOTAL RIGHT HIP ARTHROPLASTY SURGERY AT (B)(6) HOSPITAL IN (B)(6) INVOLVING THE IMPLANTATION OF THE TRIDENT DEVICE. IT WAS FURTHER REPORTED THAT, IN (B)(6) OF 2007, THE PATIENT BEGAN EXPERIENCING EXTREME PAIN AND BEGAN HEARING AUDIBLE NOISES INCLUDING SQUEAKING WHICH EMANATED FROM THE LOCATION OF HER RIGHT HIP. IT WAS FURTHER ALLEGED THAT, AS A RESULT OF THE PAIN AND SQUEAKING WHICH DEVELOPED, THE PATIENT HAS EXPERIENCED AND CONTINUES TO EXPERIENCE CONSTANT IRRITATION AND DISCOMFORT IN THE LOCATION OF HER RIGHT HIP." UPDATE AS PER MEDICAL RECORDS NOTED "ON (B)(6) 2011 A REVISION OF THE RIGHT TOTAL HIP WAS PERFORMED WITH THE PATIENT COMPLAINING OF PAIN AND SQUEAKING IN THE RIGHT TOTAL HIP."
Patient problems: Discomfort; Injury; Irritation; Pain
MAUDE report 7862134 ↗
Other Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented devices
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- BIOLOX DELTA 1365-32-320Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 death314 reports
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- 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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