DELTA TT CupRecalls & reported problems
Limacorporate SPA · Acetabular Cups (Ti6Al4V) Dia. 58mm for liner Size Large · 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 08033390040655), received between Jul 6, 2026 and Jul 6, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (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
- Patient Device Interaction Problem1
Patient problems
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 6, 2026Patient Device Interaction Problem
A HIP REVISION SURGERY WAS PERFORMED ON (B)(6) 2026 DUE TO IMPLANT LOOSENING. THE SURGEON REMOVED THE DELTA TT CUP, LINER, AND SCREWS. X-RAYS SHOWED RADIOGRAPHIC LINES AROUND THE CUP; THEREFORE, THE SURGEON EXPECTED THE IMPLANT TO COME OUT EASILY. HOWEVER, REMOVAL WITH THE EXPLANT TOOL TOOK SOME TIME, AND THE SURGEON NOTED AN IMPRESSIVE AMOUNT OF GOOD BONE IN-GROWTH/ON-GROWTH. PREVIOUS SURGERY WAS PERFORMED ON (B)(6) 2023. THE SURGEON FOLLOWED THE STANDARD SURGICAL WORKFLOW FOR HIP REVISION. THE EXPLANTED COMPONENTS INCLUDED: DELTA-TT ACETAB. CUP Ø58 MM FOR (PRODUCT CODE 5552.15.580, LOT 2202753, STER. N. (B)(4). PATIENT IS MALE. EVENT HAPPENED IN NEW ZEALAND.
Patient problems: Pain
MAUDE report 25715658 ↗
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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