Skip to content

NOVAE STICK NOVAE STICK 53Recalls & reported problems

Soc Etudes Recherches Fabrication · NOVAE Dual Mobility Acetabular Cup - NOVAE STICK metal-back cemented · Class 2 · Implant

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

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03662200005734), received between Feb 18, 2016 and Feb 18, 2016.

The most frequently reported specific device problem is “Failure To Adhere Or Bond” (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

Device problems

  • Failure To Adhere Or Bond1
  • Material Separation1

Patient problems

  • No Code Available1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • Feb 18, 2016Failure To Adhere Or Bond; Material Separation

    AFTER HE DETERMINED A HIGH INSTABILITY DURING THE OPERATION, THE SURGEON HAS CEMENTED NOVAE STICK SIZE 53 IN AN IMPLANTED ACETABULAR SHELL WHICH WAS PRELIMINARILY SEPARATED FROM ITS LINER. SHE DISLOCATED THAT CONSTRUCT (OUT THE FRONT), BECAUSE THERE WAS NOT ENOUGH ABDUCTION (CLOSURE). THE SURGEON EXPLANTED THAT ENTIRE CONSTRUCT AND RE-IMPLANTED A TM GAP CAGE WITH THIS NEW (SIZE 49) STICK FIT CUP.

    Patient problems: No Code Available

    MAUDE report 5443963 ↗

Other Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented devices

All Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented devices →

Sources and updates

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