BodyGuard Microset (2019-10-03)

Starting date:

October 3, 2019

Posting date:

November 1, 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-71443

Last updated: 2019-11-01

• 
  Reason
• 
  Affected products

Affected Products

BodyGuard Microset

Reason

When used with the BodyGuard Infusion pump system the A120-003XYVA tube set may under deliver fluid.

Affected products