Quadra H femoral stems 01.12.26SNRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07630030802669), received between Jan 20, 2020 and Jan 20, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).

1 other recall cover devices cleared under the same FDA submission (K093944, K250450); 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

Recent adverse event reports

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

• InjuryJan 20, 2020Device Dislodged or Dislocated

  THE PATIENT HAD A PRIMARY HIP SURGERY ON (B)(6) 2015. SUBSEQUENTLY, THE PATIENT CAME IN REPORTING PAIN DUE TO A FRACTURED FEMUR. THE CAUSE OF THE FRACTURE WAS UNKNOWN. THE SURGEON CABLED AND PLATED THE FRACTURE AND SURGERY WAS COMPLETED SUCCESSFULLY. PRESENTLY, ON (B)(6) 2019 (3 MONTHS AND A HALF AFTER PRIMARY) THE PATIENT CAME IN COMPLAINING OF INSTABILITY DUE TO A SUBSIDED STEM WITH NONUNION. THE CAUSE OF THE SUBSIDED STEM IS UNKNOWN. THE SURGEON REVISED THE STEM, HEAD, AND LINER AND THE SURGERY WAS COMPLETED SUCCESSFULLY.

  Patient problems: Bone Fracture(s)

  MAUDE report 9605407 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K093944, K250450. One submission often covers many models, so check the product and lot details in each record.

• Z-0791-2013 · Dec 17, 2012 · Terminated
  Medacta Quadra Trial Broach size 0 part # 01.10.10.045, for use with the Medacta Total Hip Prosthesis System. Product Usage - used to broach the intramedullary canal of the femur