Health product recall

Volumat MC Agilia CA (2019-06-25)

Starting date:
June 25, 2019
Posting date:
July 19, 2019
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-70455

Last updated: 2019-08-08

Affected Products

Volumat MC Agilia CA

Reason

Certain versions of the Volumat MC Agilia  volumetric infusion pump and vigilant drug lib software to address 4 anomalies and KVO (keep vein open) end of infusion alarm priority.

Affected products

Volumat MC Agilia CA

Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number

Z021131

Companies
Manufacturer

Fresenius Kabi AG

Else-Kröner-Straße 1

Bad Homburg vor der Höhe

61352

GERMANY