DELTA LINERS & ACCESSORIES 5885.54.259Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 08033390136105), received between Aug 29, 2025 and Mar 6, 2026 — classified as 2 injuries.

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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryMar 6, 2026Insufficient Device Problem Information

  REVISION SURGERY OF HIP PROSTHESIS WAS PERFORMED ON (B)(6) 2026 DUE TO UNKNOWN REASON. ORIGINAL SURGERY OCCURRED ON (B)(6) 2023 TO IMPLANT THE FOLLOWING COMPONENTS: - DELTA TT ACETABULAR CUP DIA52MM (PN 5553.14.523, LOT 2216711, STERILIZATION (B)(4)) - DELTA NEUTRAL LINER #MEDIUM (PN 5885.54.259, LOT 2112535, STERILIZATION (B)(4)) - MASTERSL LATERALIZED HIP STEM (PN 3516.21.220, LOT 2221511, STERILIZATION (B)(4)) - BIOLOX DELTA FEMORAL HEAD MEDIUM TAPER=12/14 (PN 5010.42.362, LOT 2283891, STERILIZATION (B)(4)). DURING REVISION THE SURGEON REPLACED THE PRE-EXISTING LINER WITH A NEW ONE (PN 5887.54.259). SURGERY WAS COMPLETED AS INTENDED. THE PATIENT IS FEMALE, DATE OF BIRTH (B)(6) 1943. THE EVENT OCCURRED IN THE UNITED STATES.

  Patient problems: Insufficient Information

  MAUDE report 24531029 ↗
• InjuryAug 29, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated

  REVISION SURGERY PERFORMED ON (B)(6) 2025, DUE TO DISLOCATION. THE FOLLOWING COMPONENTS WERE REMOVED: - DELTA TT PRO D.52MM MEDIUM+ (PART CODE 5553.14.523, LOT NUMBER 2333067, STERILIZATION (B)(4)). - DELTA NEUTR. LINER D.36MM #M+ (PART CODE 5885.54.259, LOT NUMBER 24AT0A7, STERILIZATION (B)(4)). - BONE SCREW Ø6,5 H.30MM (PART CODE 8420.15.030, LOT NUMBER 2509960, STERILIZATION (B)(4)). THESE COMPONENTS WERE REPLACED BY THE FOLLOWING NEW ONES: - DELTA TT CUP D.54MM (PART CODE 5552.15.540, LOT NUMBER 2304688, STERILIZATION (B)(4)). - DELTA MOBILE LINER (PART CODE 5566.50.420, LOT NUMBER 20AT0Y8, STERILIZATION (B)(4)). - BONE SCREW DIA=6.5MM H=25MM (PART CODE 8420.15.020, LOT NUMBER 2411118, STERILIZATION (B)(4)). - BONE SCREW DIA=6.5MM H=35MM (PART CODE 8420.15.040, LOT NUMBER 2201892, STERILIZATION (B)(4)). - DELTA CUP DUAL MOBILITY LINER #LARGE (PART CODE 5885.09.042, LOT NUMBER 2017046, STERILIZATION (B)(4)). PREVIOUS SURGERY WAS PERFORMED ON (B)(6) 2025. THE PATIENT IS A MALE, DATE OF BIRTH (B)(6)1953. THE EVENT HAPPENED IN THE UNITED STATES.

  Patient problems: Joint Dislocation

  MAUDE report 22922803 ↗