Events

Recall of VISIONS FIVE/64 F/X

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by VOLCANO CORPORATION.

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
    63909
  • Event Risk Class
    III
  • Event Initiated Date
    2015-10-21
  • 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
    June 4 2015 volcano corporation recalled lot #50002518 visions pv.035 catheter (all s/n 0232 50002518xxx) and lot #50004551 prestige plus 185 cm j-tip (s/n 0111 50004551xxx and xxx = 005-060) due to incorrect expiry date printed on the package which is beyond its expiration date.

Device

VISIONS FIVE/64 F/X
  • Model / Serial
    Model Catalog: 88901 (Lot serial: 50002518 S/N- All); Model Catalog: 9185J (Lot serial: 50004551 S/N 005-060)
  • Product Description
    PV.035 Catheter
  • Manufacturer
    VOLCANO CORPORATION

Manufacturer

VOLCANO CORPORATION
  • Manufacturer Address
    RANCHO CORDOVA
  • Manufacturer Parent Company (2017)
    Philips
  • Source
    HC