Delta Dual Mobility System 5566.50.420Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 08033390012447), received between Oct 9, 2024 and Oct 9, 2024 — classified as 1 injury.

The most frequently reported specific device problem is “Degraded” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryOct 9, 2024Degraded; Degraded

  HIP REVISION SURGERY PERFORMED ON (B)(6) 2024, DUE TO WEAR OF THE MOBILE LINER ØINT 28 MM Ø42 MM (PRODUCT CODE 5566.50.420, LOT #1316292 - STER. 1400084). ACCORDING TO THE RECEIVED INFORMATION, THE PATIENT FELT STIFFNESS AND LOSS OF RANGE OF MOTION, AND THE PATIENT WENT FOR A CHECKUP. SHE HAD PAIN FOR A COUPLE OF WEEKS. IT WAS REPORTED THAT SINCE THE SURGEON IMPLANTED A LIMA DUAL MOBILITY LINER INTO A COMPETITOR'S CUP (OFF LABEL PROCEDURE), THE POLY LINER WORN DOWN OVER TIME. THE FOLLOWING DEVICES WERE EXPLANTED: · MOBILE LINER ØINT 28 MM Ø42 MM (PRODUCT CODE 5566.50.420, LOT #1316292 - STER. 1400084) · FEMORAL MODULAR HEAD - M Ø28MM (PRODUCT CODE 5010.42.282, LOT #1480074 - STER. 1400030) THE SURGEON REPLACED THE WORN LINER WITH A NEW COMPETITOR'S LINER AND A SLEEVE AND HEAD FROM ANOTHER COMPETITOR. THE FEMORAL COMPONENTS (LIMA'S REVISION STEM AND NECK) REMAINED IN SITU. PREVIOUS SURGERY TOOK PLACE ON (B)(6) 2014 (IT WAS A PRIMARY). PATIENT IS A FEMALE, 52 YEARS OLD. NO COMORBIDITIES ARE KNOWN. EVENT HAPPENED IN AUSTRALIA.

  Patient problems: Limb Pain; Loss of Range of Motion

  MAUDE report 20406645 ↗