Events

Recall of N LATEX FLC KAPPA/LAMBDA

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
    19930
  • Event Risk Class
    III
  • Event Initiated Date
    2015-03-24
  • 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
    Siemens healthcare diagnostics has received customer complaints about qc recovery for parameter "free ig/l-chain type lambda" using several n latex fls lambda reagent / n flc control sl1 and n flc control sl2 combination on bn prospec system. controls were measured outside the upper limit of the confidence range. manufacturer has confirmed a higher than than expected rate of invalid runs.

Device

N LATEX FLC KAPPA/LAMBDA
  • Model / Serial
    Model Catalog: 10482442 (Lot serial: > 10 LOT #S CONTACT MFR); Model Catalog: 10482441 (Lot serial: > 10 LOT #S CONTACT MFR); Model Catalog: 10482440 (Lot serial: > 10 LOT #S CONTACT MFR)
  • Product Description
    N LATEX FLC KAPPA/LAMBDA
  • Manufacturer
    SIEMENS HEALTHCARE LIMITED

Manufacturer

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