Events

Recall of FLEXIBLE HUMERAL NAIL SYSTEM

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
    22142
  • Event Risk Class
    II
  • Event Initiated Date
    1998-11-17
  • Event Country
    Canada
  • 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
    The central wire may be undersized which could cause it to disengage during removal.

Device

FLEXIBLE HUMERAL NAIL SYSTEM
  • Model / Serial
    Model Catalog: (Lot serial: 475.050 AND 475.242 TO 475.250); Model Catalog: (Lot serial: PART NUMBERS 475.042 TO); Model Catalog: (Lot serial: ALL LOT NUMBERS)
  • Product Description
    TI FLEXIBLE HUMERAL NAIL
  • Manufacturer
    SYNTHES (CANADA) LTD.

Manufacturer

SYNTHES (CANADA) LTD.
  • Manufacturer Address
    MISSISSAUGA
  • Manufacturer Parent Company (2017)
    Johnson & Johnson
  • Source
    HC