Events

Recall of ADVIA 2120 WITH AUTOSAMPLER

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

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
    57324
  • Event Risk Class
    III
  • Event Initiated Date
    2011-09-14
  • 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
    Customer complaint received that during troubleshooting a syringe filled with ez kleen was connected to the perox 2 reagent tubing. the ez kleen sprayed onto the operator's forehead after the syringe plunger caused the tygon tubing to disconnect at the check valve.

Device

ADVIA 2120 WITH AUTOSAMPLER
  • Model / Serial
    Model Catalog: 10316162 (Lot serial: ); Model Catalog: 10361803 (Lot serial: ); Model Catalog: 10317457 (Lot serial: ); Model Catalog: 10315687 (Lot serial: ); Model Catalog: 10361798 (Lot serial: ); Model Catalog: 10313419 (Lot serial: ); Model Catalog: 10310973 (Lot serial: )
  • Product Description
    ADVIA 2120 WITH AUTOSAMPLER
  • Manufacturer
    SIEMENS HEALTHCARE LIMITED

Manufacturer

SIEMENS HEALTHCARE LIMITED
  • Manufacturer Address
    OAKVILLE
  • Manufacturer Parent Company (2017)
    Siemens Ag
  • Source
    HC