DJO SURGICAL 498-32-052Recalls & reported problems
Encore Medical, L.P. · Ceramic Liner - Size 32 · Class 3 · Implant
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 00888912087599), received between Oct 12, 2016 and Jan 13, 2020 — classified as 4 injuries.
The most frequently reported specific device problem is “Crack” (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
- Appropriate Device Problem Term/Code Not Available1
- Crack1
- Failure To Adhere Or Bond1
- Fracture1
Patient problems
- No Code Available2
- 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.
InjuryJan 13, 2020Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - PATIENT UNDERGOES REMOVAL OF RIGHT HIP AND PLACEMENT OF ANTIBIOTIC SPACER. "GROSS PURULENCE" OBSERVED IN RIGHT HIP WHICH CAUSED SURGEON TO DECIDE TO REMOVE THE (ENCORE) HIP COMPONENTS AND PLACE AN ANTIBIOTIC SPACER. THE OPERATIVE REPORT DOES NOT REFLECT THE FINDING OF ANY PSEUDOTUMOR.
Patient problems: No Information
MAUDE report 9581587 ↗InjuryFeb 4, 2019Fracture
REVISION SURGERY - DUE TO A FRACTURE ON THE LINER. THE SURGEON REMOVED AND REPLACED THE ORIGINAL LINER AND HEAD.
Patient problems: No Code Available
MAUDE report 8301274 ↗InjuryMay 25, 2018Crack
REVISION SURGERY - DUE TO THE CERAMIC LINER HAVING CRACKED. THE SURGEON TOOK OUT ALL ORIGINAL COMPONENTS EXCEPT THE STEM.
Patient problems: Failure of Implant
MAUDE report 7545932 ↗InjuryOct 12, 2016Failure To Adhere Or Bond
REVISION SURGERY - THE PATIENT HAD A RIGHT TOTAL HIP ARTHROPLASTY ON (B)(6) 2001. IT WAS A KERAMOS-CERAMIC ON CERAMIC HIP IMPLANT. DUE TO THE ACETABULAR CUP HAVING BECOME LOOSE; THE CERAMIC LINER, ACETABULAR SHELL, AND SCREW WERE ALL REMOVED, AS WELL AS THE CERAMIC FEMORAL HEAD. THE SURGEON REPLACED THE ACETABULAR COMPONENTS WITH ZIMMER PRODUCTS AND PUT IN A NEW DJO SURGICAL COCR FEMORAL HEAD.
Patient problems: No Code Available
MAUDE report 6023993 ↗
Other Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented devices
- BIOLOX DELTA 1365-36-310Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented839 reports
- BIOLOX DELTA 1365-36-320Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented643 reports
- PINNACLE POROCOAT 1217-22-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented335 reports
- PINNACLE POROCOAT 1217-22-054Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented263 reports
- BIOLOX DELTA 1365-36-330Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented255 reports
- PINNACLE POROCOAT 1217-22-050Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented253 reports
- PINNACLE POROCOAT 1217-22-056Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented220 reports
- SUMMIT POROCOAT 1570-11-120Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented1 death204 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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