Events

Recall of RABBIT ANTI-PNEUMOCYSTIS CARINII CLONE 3F6

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by DAKO DENMARK A/S.

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
    76898
  • Event Risk Class
    II
  • Event Initiated Date
    2018-03-23
  • 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
    The primary labels of the affected vials of m0778 and m0880 were mislabeled with an incorrect concentration. for m0778 the concentration was written to be 30 mg/l. the correct concentration is 75 mg/l. for m0880 the concentration was written to be 187 mg/l. the correct concentration is 485 mg/l.

Device

RABBIT ANTI-PNEUMOCYSTIS CARINII CLONE 3F6
  • Model / Serial
    Model Catalog: M0778 (Lot serial: 20042555); Model Catalog: M0778 (Lot serial: 20010445); Model Catalog: M0778 (Lot serial: 20030858)
  • Product Description
    MONOCLONAL MOUSE ANTI-PNEUMOCYSTIS JIROVECI CLONE 3F6
  • Manufacturer
    DAKO DENMARK A/S

Manufacturer

DAKO DENMARK A/S