DELTA TT Pro 5553.14.503Recalls & reported problems
Limacorporate SPA · Acetabular Cup (Ti6Al4V) Dia. 50 mm, for Liners size MEDIUM + · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 08033390146043), received between Jan 2, 2026 and Jan 2, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Loss of or Failure to Bond” (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.
Reports received per month
Most reported problems
Device problems
- Loss of or Failure to Bond1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 2, 2026Loss of or Failure to Bond
REVISION SURGERY WAS PERFORMED ON (B)(6) 2025 DUE TO NON UNION OF THE HIP PROSTHESIS. ACCORDING TO INFORMATION PROVIDED BY COMPLAINT SOURCE, THE PERFORMANCE ISSUE WAS REPORTED ON THE ACETABULAR SIDE OF THE PROSTHETIC ASSEMBLY. PREVIOUS SURGERY WAS PERFORMED ON (B)(6) 2021, AND FOLLOWING COMPONENTS WERE IMPLANTED: DELTA TT PRO D50MM MEDIUM+ ACETABULAR CUP (PART NUMBER 5553.14.503, LOT 2117019, STERILIZATION 2100278), DELTA NEUTRAL LINER D36MM #M (PART NUMBER 5885.54.259, LOT 2107883, STERILIZATION 2100206), MASTER SL STEM #5 (PART NUMBER 3515.21.250, LOT 2022664, STERILIZATION 2100029), FEMORAL MODULAR HEAD S - DIA36MM (PART NUMBER 5010.42.361, LOT 2183087, STERILIZATION 2100217). DURING REVISION SURGERY, THE LIMA PROSTHETIC COMPONENTS WERE EXPLANTED AND REPLACED WITH EMPOWR ACETABULAR SYSTEM AND BONE SCREWS. ALSO THE CERAMIC FEMORAL HEAD HAS BEEN REPLACED WITH THE EMPOWR ONE FOR COMPATIBILITY REASONS, WHILE THE FEMORAL STEM REMAINED IN PLACE SINCE NO PROBLEMS WITH THAT COMPONENT WERE FOUND BY SURGEON. SURGERY HAS BEEN COMPLETED AS INTENDED. PATIENT IS MALE, DATE OF BIRTH (B)(6) 1951. THE EVENT OCCURRED IN THE UNITED STATES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23942996 ↗
Other Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented devices
- PINNACLE 1217-25-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED735 reports
- NA 1365-52-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED683 reports
- APEX 1246-03-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED3 deaths613 reports
- PINNACLE 1217-20-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 deaths590 reports
- PINNACLE 1217-30-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 death484 reports
- NA 1365-53-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED404 reports
- PINNACLE ALTRX 1221-36-054Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED388 reports
- PINNACLE ALTRX 1221-32-050Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED386 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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