Health product recall

BD Bodyguard Microset

Last updated

Summary

Product
BD Bodyguard Microset
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalogue number

BD Bodyguard Microset

More than 10 numbers, contact manufacturer.

120-160XCSK

Issue

BD received customers complaints, that the new clamp on the y-port of the BD Bodyguard™ Microset (clamp supplied since 2021) can be opened more easily compared to the clamp which was used before 2021. Patients may accidentally lay on the infusion set and unintentionally open the clamp causing the infusion set to be exposed to atmospheric air/ environment, if a vented clamp is being used. The longer this failure mode remains undetected the higher the potential volume of air entry.

Recall start date: February 26, 2024

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies
Caesarea Medical Electronics Ltd.
16 Shacham Street, Caesarea, Israel, 3088900
Published by
Health Canada
Audience
Healthcare
Recall class
Type I
Identification number
RA-75184

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