Public recall detail

Bililux

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Recall Safety notice
Quick summary

Quick summary: Bililux.

Recommended action

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Recall details

Quick summary: Bililux.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandDraeger Medical Systems, Inc.
ProductBililux
IssueMedical devices - Manufacturing defect
Recall classType II
IdentificationRA-64156

Affected products

ProductBililux
LotMore than 10 numbers, contact manufacturer.
ModelMU20100
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionBililux

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

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceGeneral public Health professionals Hospitals
CategoryHealth products - Medical devices - General hospital and personal use
CompaniesDraeger Medical Systems, Inc. 3135 Quarry Road, Telford, Pennsylvania United States, 18969
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-64156
Background{}
CompaniesDraeger Medical Systems, Inc. 3135 Quarry Road, Telford, Pennsylvania United States, 18969
AudiencesGeneral public Health professionals Hospitals
Source updated2022-05-10

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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