Events

Recall of ALLSET GOLD SSP HLA DIRECT TO HIGH RESOLUTION KITS

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by LIFE TECHNOLOGIES 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
    41375
  • Event Risk Class
    III
  • Event Initiated Date
    2013-02-25
  • 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
    Complaint states the opb1 ssp aiiset gold kit has a false negative in lane 39 which gives no perfect match typing result for the opb 1 *135:01 allele. internal investigation has confirmed with the now available rare sample type that it is lane 27 which is negative for the opb 1 *135:01 allele not lane 39 in the above listed affected kits according to the labeling provided with the kits. the primer mixes had not been tested with a opb1 *135:01 sample.

Device

ALLSET GOLD SSP HLA DIRECT TO HIGH RESOLUTION KITS
  • Model / Serial
    Model Catalog: 54070D (Lot serial: 008 1127336); Model Catalog: 54070D (Lot serial: 008 1204422); Model Catalog: 451616D (Lot serial: > 10 contact manufacturer)
  • Product Description
    AIISet Gold SSP HLA-DPB1 High Res Kit
  • Manufacturer
    LIFE TECHNOLOGIES CORPORATION

Manufacturer

LIFE TECHNOLOGIES CORPORATION