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