Health product recall

MOSAIQ (2018-08-03)

Starting date:
August 3, 2018
Posting date:
August 17, 2018
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-67448

Affected products

MOSAIQ

Reason

Leaving the Medication Administration Record (MAR) window open when navigating to the Clinician Worksheet (CWS) can leave the order status in an incorrect state.

Affected products

MOSAIQ

Lot or serial number

2.64 SP3 or higher

Model or catalog number

MOSAIQ

Companies
Manufacturer

Elekta Inc.

100 Mathilda Place

Sunnyvale

94086

California

UNITED STATES