Bodyguard Microset (2020-01-14)

Starting date:

January 14, 2020

Posting date:

April 15, 2020

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-72717

Last updated: 2020-05-01

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  Reason
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  Affected products

Affected Products

Bodyguard Microset

Reason

Filter installed onto the tube set may have the incorrect pore size (0.2 micron vs 1.2 micron).

Affected products