Events

Recall of CELLINE 10L POLYPAC

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

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
    34674
  • Event Risk Class
    III
  • Event Initiated Date
    2008-07-24
  • 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
    Complaint that the product had an incorrect expiry date. on label was april 31 2009 where it should have read april 30 2009. material is confirmed to be within specs and no copromise in product quality and inte.

Device

CELLINE 10L POLYPAC
  • Model / Serial
    Model Catalog: 35114210 (Lot serial: SC8079267)
  • Product Description
    celline 10l polypac
  • Manufacturer
    FISHER SCIENTIFIC

Manufacturer

FISHER SCIENTIFIC