Health product recall

MOSAIQ

Last updated

Summary

Product
MOSAIQ
Issue
Medical devices - Performance
What to do

A field safety notice will be sent. A field safety modication will follow. 

Audience
Healthcare

Affected products

Affected products Lot or serial number Model or catalogue number
MOSAIQ 3.2.1 3.2.1.0 (01)07340201500071(10)3.2.1.0
MOSAIQ 3.2.1 3.2.1.1 (01)07340201500071(10)3.2.1.1
MOSAIQ 3.2.1 3.2.1.2 (01)07340201500071(10)3.2.1.2
MOSAIQ 3.2.1 3.2.1.3 (01)07340201500071(10)3.2.1.3
MOSAIQ 3.2.1 3.2.1.4 (01)07340201500071(10)3.2.1.4
MOSAIQ 3.1.3 3.1.3.0 (01)07340201500026(10)3.1.3.
MOSAIQ 3.1.3 3.1.3.1 (01)07340201500026(10)3.1.3.1
MOSAIQ 3.1.3 3.1.3.2 (01)07340201500026(10)3.1.3.2
MOSAIQ 3.1.3 3.1.3.3 (01)07340201500026(10)3.1.3.3
MOSAIQ 3.1.3 3.1.3.4 (01)07340201500026(10)3.1.3.4
MOSAIQ 3.2.2 3.2.2.0 (01)07340201500071(10)3.2.2.0
MOSAIQ 3.2.2 3.2.2.1 (01)07340201500071(10)3.2.2.1
MOSAIQ 3.2.3.0 3.2.3.0 (01)07340201500071(10)3.2.3.0

Issue

When appending a care plan with an ad hoc waved order set, if an order does not fall on a care plan cycle day, it is not appended.  If the care plan is not appended, it may result in one or more doses of the medication(s) not being administered.

Recall start date: August 29, 2025

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies
Elekta Solutions Ab
Hagaplan 4, Stockholm, Sweden, 11368
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-78024

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