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Active Articulation™ Dual Mobility Hip System XL-200156Recalls & reported problems

Biomet Orthopedics, LLC · Class 2 · Implant

All models of Active Articulation Dual Mobility Hip System (5)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00880304491380), received between Jul 12, 2021 and Nov 11, 2021 — classified as 2 injuries.

2 other recalls cover devices cleared under the same FDA submission (K110555, K161190); they may or may not involve this specific model.

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

Device problems

  • Adverse Event Without Identified Device or Use Problem2

Patient problems

  • Inflammation1
  • Pain1
  • Scar Tissue1
  • Unspecified Infection1

Recent adverse event reports

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

  • InjuryNov 11, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT PATIENT UNDERWENT AN ENDOSCOPIC PROCEDURE APPROXIMATELY ELEVEN(11) YEARS POST IMPLANTATION TO REMOVE SCAR TISSUE, RELEASE RIGHT HIP FLEXOR TENDON & REMOVE BURSA. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

    Patient problems: Inflammation; Pain; Scar Tissue

    MAUDE report 12797727 ↗
  • InjuryJul 12, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

    Patient problems: Unspecified Infection

    MAUDE report 12149647 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K110555, K161190. One submission often covers many models, so check the product and lot details in each record.

  • Z-1024-2017 · Dec 19, 2016 · Terminated
    RingLoc ArComXL Highly Crosslinked Polyethylene Liners ArComXL High Wall +3mm Liners Size 23 item XL-108323 ArComXL MaxRom +3mm Liners Size 23 item XL-108223
  • Z-1025-2017 · Dec 19, 2016 · Terminated
    Active Articulation ArComXL Polyethylene Bearings Active Articulation ArComXL Bearings item XL-200152

Other Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented devices

All Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page