ProductGuru Recalls

Official recall record

MOSAIQ (ref 78024)

Health Canada — Medical Devices · 2025-09-04 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2025-09-04
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

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

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

More recalls: Health Canada — Medical Devices · Canada · all filters

ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.