Rappel de produits de santé

MaxPlus Needleless Connector (2019-04-29)

Starting date:
April 29, 2019
Posting date:
May 10, 2019
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-69900



Last updated: 2019-05-10

Affected Products

MaxPlus Needleless Connector

Reason

The recall is being conducted due to a lot specific defect, where after disconnection of a luer, the valve of the connector remains recessed; not fully closing, either temporarily or permanently. The risks of blood loss and air embolism exist if the valve remains permanently open and goes undetected, especially in the neonate population.

Affected products

MaxPlus Needleless  Connector

Lot or serial number
  • 18085990
Model or catalog number
  • MP1000-C
Companies
Manufacturer

BD Switzerland SARL

Route de Crassier 17, Business Park Terre Bonne

Eysins

1262

SWITZERLAND