Events

Recall of Smith & Nephew Birmingham Hip Modular Head (BHMH)

According to New Zealand Medicines and Medical Devices Safety Authority, this recall involved a device in New Zealand that was produced by Smith & Nephew Orthopaedics Ltd.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    13530
  • Event Initiated Date
    2012-10-02
  • Event Country
    New Zealand
  • Event Source
    NZMMDSA
  • Event Source URL
    https://medsafe.govt.nz/hot/Recalls/RecallSearch.asp
  • Notes / Alerts
    Data from New Zealand is current through July 2018. All of the data comes from the New Zealand Medicines and Medical Devices Safety Authority, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and New Zealand.
  • Extra notes in the data
    Recalling Organisation: Smith & Nephew Surgical Ltd, Unit A 36 Hillside road, Wairau Valley, AUCKLAND 0760
  • Reason
    Following reports of higher than expected revision rates the manufacturer has discontinued use of this device as a primary for total hip replacements. use has been restricted to revisions only in conjunction with the s&n synergy femoral stem.
  • Action
    Manufacturer to issue advice regarding use

Device

Smith & Nephew Birmingham Hip Modular Head (BHMH)

Manufacturer

Smith & Nephew Orthopaedics Ltd