Events

Safety Alert for Microbore Administration Set and Epidural Administration Set

According to Department of Health, this safety alert involved a device in Hong Kong that was produced by Moog Medical Devices Group.

What is this?

Alerts provide important information and recommendations about products. Even though an alert has been issued, it does not necessarily mean a product is considered to be unsafe. Safety Alerts, addressed to health workers and users, may include recalls. They can be written by manufacturers, but also by health officials.

Learn more about the data here
  • Type of Event
    Safety alert
  • Date
    2012-06-08
  • Event Date Posted
    2012-06-08
  • Event Country
    Hong Kong
  • Event Source
    DH
  • Event Source URL
    https://www.mdco.gov.hk/english/safety/recalls/recalls_20120608b.html
  • Notes / Alerts
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), 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 data from the U.S. and Hong Kong.
  • Extra notes in the data
    Medical Device Safety Alert
  • Reason
    Medical device safety alert: moog microbore administration set and epidural administration set the united states food and drug administrations (fda) has issued a class i recall concerning non-dehp microbore administration set and epidural administration set (model no: 340-4114, 340-4115, 340-4126, 340-4128, 340-4128-v, 340-4130, 340-4130-v, 340-4137, 340-4144, 340-4165, 340-4166, 340-4173, 340-4133, 340-4176), manufactured by moog medical devices group. the manufacturer became aware via customer complaint, of a reversed pump segment on an administration set. this malfunction could reverse the flow of fluid or medication backwards from what was intended. for details, please refer to fda website http://www.Fda.Gov/safety/recalls/enforcementreports/ucm307229.Htm if you are in possession of the product, please contact your supplier for necessary actions. posted on 8 june 2012.

Device

Microbore Administration Set and Epidural Administration Set
  • Model / Serial
  • Product Description
    Medical Device Safety Alert: Moog Microbore Administration Set and Epidural Administration Set
  • Manufacturer
    Moog Medical Devices Group

Manufacturer

Moog Medical Devices Group
  • Manufacturer Parent Company (2017)
    Moog Inc
  • Source
    DH