Recall of PUSH-PULL REDUCTION DEVICE

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by SYNTHES (CANADA) 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
    31115
  • Event Risk Class
    II
  • Event Initiated Date
    2015-06-04
  • Event Country
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Extra notes in the data
  • Reason
    Synthes (canada) ltd. received notification from its supplier synthes (usa) that a determination had been made that a voluntary recall would be performed as it was reported the affected part and lots of the pull reduction device may have been manufactured to an incorrect hardness specification which could result in intra-operative breakage.

Device

  • Model / Serial
    Model Catalog: 03.120.023 (Lot serial: 3172147); Model Catalog: 03.120.023 (Lot serial: 3159152); Model Catalog: 03.120.023 (Lot serial: 3139483); Model Catalog: 03.120.023 (Lot serial: 3139480); Model Catalog: 03.120.023 (Lot serial: 3052800)
  • Product Description
    PUSH-PULL REDUCTION DEVICE
  • Manufacturer

Manufacturer

  • Manufacturer Address
    MISSISSAUGA
  • Manufacturer Parent Company (2017)
  • Source
    HC