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Contour 71337156Recalls & reported problems

Smith & Nephew, Inc. · CONTOUR ACETABULAR RECONSTRUCTION RING 56MM OUTER DIAMETER 52MM INNER DIAMETER LEFT · Class 2 · Implant

Adverse event reports
3
Deaths reported
0
Injuries reported
3
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 03596010308290), received between Sep 17, 2018 and Jun 24, 2019 — classified as 3 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (2 reports).

1 other recall cover devices cleared under the same FDA submission (K211176, K962541); 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Insufficient Device Problem Information2
  • Fracture1

Patient problems

  • Unspecified Infection2
  • Injury1

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • InjuryJun 24, 2019Fracture; Fracture

    IT WAS REPORTED THAT THE FLAP FRACTURE OF THE ACETABULAR RING, RESULTING IN LOOSENING OF THE IMPLANT.

    Patient problems: Injury

    MAUDE report 8727961 ↗
  • InjurySep 26, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

    IT WAS REPORTED A REVISION SURGERY DUE TO INFECTION. PATIENT HAD RECENTLY A SECOND REVISION FOR INFECTION ON SAME HIP. UNFORTUNATELY THE PATIENTS INFECTION PROGRESSED LEADING TO TODAY'S 3RD REVISION. HEAD PUNCHED OFF STEM. STEM REMOVED WITH PROXIMAL CEMENT PLUG ALL POLY CUP REMOVED WITH RENOVATION INSTRUMENTS SCREWS X 7 REMOVED AND CONTOUR CAGE REMOVED (71337156). NO LOT NUMBER IDENTIFIABLE CAGE REMOVED. UNDERLYING MESH WAS OVERGROWN BY BONE SO LEFT IN SITU.

    Patient problems: Unspecified Infection

    MAUDE report 7909523 ↗
  • InjurySep 17, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

    IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED TO REPLACE IMPLANTS STRYKER ALL POLY CUP, CPCS STEM AND HEAD DUE TO INFECTION.

    Patient problems: Unspecified Infection

    MAUDE report 7881001 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K211176, K962541. One submission often covers many models, so check the product and lot details in each record.

  • Z-0326-2025 · Oct 15, 2024 · Open, Classified
    Tandem Intl Bipolar Cocr Shell/UHMWPE Liner, TI-6AL-4V Retaining Ring, 28MM I.D. 46 MM O.D., REF 71324046, sterile, femoral head bipolar component of the Tandem Bipolar Hip System.

Other Mesh, surgical, acetabular, hip, prosthesis devices

All Mesh, surgical, acetabular, hip, prosthesis devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.