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Plum Infusion Pumps (2016-03-30)
- Starting date:
- March 30, 2016
- Posting date:
- April 15, 2016
- 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-57956
Affected Products
A. Plum A+ Infusion Pump
B. Plum 360 Infusion Pump
Reason
Some Plum 360 and Plum A+ infusion pumps were not properly calibrated during the manufacturing process. As a result, the impacted pumps can potentially produce false proximal occlusion alarms during cassette initialization (set-up of the therapy) or the alarm may be delayed in the case of a proximal occlusion during delivery (therapy).
Affected products
A. Plum A+ Infusion Pump
Lot or serial number
More than 10 numbers, contact manufacturer.
Model or catalog number
20792-13
20792-65
Companies
- Manufacturer
-
Hospira Inc.
275 North Field Drive
Lake Forest
60045
Illinois
UNITED STATES
B. Plum 360 Infusion Pump
Lot or serial number
More than 10 numbers, contact manufacturer.
Model or catalog number
30010-13
30010-65
Companies
- Manufacturer
-
Hospira Inc.
275 North Field Drive
Lake Forest
60045
Illinois
UNITED STATES