Plum 360 Infusion Pump

Starting date:
January 4, 2017
Posting date:
January 10, 2017
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type I
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-61738

Reason

When the AC power is lost and quickly resumed, the pump software incorrectly classifies the event as an e323 alarm condition resulting in an interruption of any ongoing therapy.  If this issue occurs the pump requires manual user input to resume previous infusion.

Affected products

Plum 360 Infusion Pump

Lot or serial number

Software Version 15.02

Model or catalog number

30010

Companies

Manufacturer
Hospira Inc.
275 North Field Drive
Lake Forest
60045
Illinois
UNITED STATES