Recall of STATIM 7000 CASSETTE STERILIZER

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by SCICAN 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
    105113
  • Event Risk Class
    III
  • Event Initiated Date
    2015-01-20
  • 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
    This recall has been initiated due to a part that is no longer available. this part is an rfid (radio-frequency identification) tag which is used in the chamber seal to monitor the number of cycles ran in order to inform the user when it is necessary to change the chamber seal. our current supplier of this part has decided to exit the rfid tag business and a suitable replacement was not found. therefore all future cassette seals will no longer contain the rfid tag (seals are regularly replaced by the user). when this tag ?s not present the machine will not allow a cycle to start with the current software. ln order to implement this change in the stat/m 7000 and remove the rfid tag from the cassette seal the rfid board software must be updated to allow the unit to run without an rfid tag in the cassette seal. this will be performed by trained technicians at the user site. there is no need for the unit to be returned to the manufacturer for this software update. the life of the seal is still 1000 cycles or every twelve months whichever comes first but no notification will be given on the unit once the tag is no longer present and the software has been updated. it will be the user's responsibility to monitor the number of cycles ran and the seal's performance. manual monitoring of seal replacement is a common practice for most steam sterilizers on the market.

Device

  • Model / Serial
    Model Catalog: 01-702100 (Lot serial: >10 contact mfg.); Model Catalog: 01-702101 (Lot serial: >10 contact mfg.); Model Catalog: 01-702101-R (Lot serial: >10 contact mfg.); Model Catalog: 01-702101-L (Lot serial: >10 contact mfg.)
  • Product Description
    STATIM 7000 CASSETTE STERILIZER
  • Manufacturer

Manufacturer

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