Bililux
Brand(s)
Last updated
Summary
Product
Bililux
Issue
Medical devices - Manufacturing defect
What to do
Contact the manufacturer if you require additional information.
Affected products
Affected Products |
Lot or Serial Number |
Model or catalog number |
|---|---|---|
Bililux |
More than 10 numbers, contact manufacturer. |
MU20100 |
Issue
During continuous post market surveillance, Draeger gathered information and market feedback indicating that there is a need to provide additional information in the instructions for use regarding the potential of the user to incorrectly position the Bililux spring arm. The incorrect positioning of the spring arm could in rare occurrences allow for the arm to move forward or down.
Recall start date: May 4 , 2022
Additional information
Details
Original published date: 2022-05-12
Alert / recall type
Health product recall
Category
Health product - Medical device - General hospital and personal use
Companies
Draeger Medical Systems, Inc.
3135 Quarry Road, Telford, Pennsylvania
United States, 18969
Published by
Health Canada
Audience
General public
Health professionals
Hospitals
Recall class
Type II
Identification number
RA-64156