DELTA CUP ACCESSORIES Protruded LinerRecalls & reported problems
Limacorporate SPA · Protruded Liners (UHMWPE X-LIMA + Ti6Al4V) I.D. 28mm - Size SMALL · 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 08033390041133), received between Nov 8, 2024 and Nov 8, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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
- Adverse Event Without Identified Device or Use Problem1
- Device Dislodged or Dislocated1
Patient problems
- Implant Pain1
- Joint Dislocation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 8, 2024Device Dislodged or Dislocated; Adverse Event Without Identified Device or Use Problem; Device Dislodged or Dislocated; Adverse Event Without Identified Device or Use Problem
HIP REVISION SURGERY PERFORMED ON (B)(6) 2024 DUE TO CUP LUXATION. ACCORDING TO THE COMPLAINT SOURCE DURING REVISION SURGERY THE PE INSERT APPEARED DISSOCIATED AND ROTATED. DURING WHICH NEW LINER, FEMORAL HEAD AND A DELTA TT CUP FIXED WITH A SCREW WERE IMPLANTED. PREVIOUS SURGERY PERFORMED ON (B)(6) 2024, AFTER WHICH THE PATIENT COMPLAINT PERSISTING PAIN FOR WHICH PAIN KILLERS WERE PRESCRIBED. POST-OPERATIVE FOLLOW-UP X-RAYS WERE PERFORMED, AND IT WAS DETECTED CRANIAL DISLOCATION OF THE FEMORAL COMPONENT OF THE ARTHROPLASTY, REDUCED THEN BY THE OPERATOR IN THE INPATIENT ROOM. EXPLANTED DEVICES DURING SURGERY: · DELTA PROTR.LINER ØINT 28MM #S (PRODUCT CODE: 5886.51.055, LOT. 2225560 - STER. 2200302). · FEM. MODULAR HEAD - L Ø28MM (PRODUCT CODE: 5010.42.283, LOT. 7011821890). · DELTA-TT ACETAB.CUP Ø48 MM FOR (PRODUCT CODE: 5552.15.480, LOT. 2011910 - STER. 2000279). DEVICE MINIMA S STANDARD STEM #1 (PRODUCT CODE: 4503.21.010, LOT: 2316595 - STER. 2300203) HAS REMAINED IN SITU. PATIENT: FEMALE, 59 YEARS OLD, APPROXIMATE HEIGHT (M) 1.61, APPROXIMATE WEIGHT (KG) 53, ACTIVE ACTIVITY LEVEL, NO SMOKING AND A HEALTHY LIFESTYLE. EVENT OCCURRED IN ITALY.
Patient problems: Implant Pain; Joint Dislocation
MAUDE report 20639157 ↗
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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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