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Plum Infusion Pumps (2015-02-05)
- Starting date:
- February 5, 2015
- Posting date:
- February 16, 2015
- 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-43741
Recalled Products
A) Plum A+ Volumetric Infusion Pump
B) Plum A+3 Infusion Pumps
Reason
Hospira is issuing this safety notification to provide clarification wording for the technical service manuals of the plum A+/A+3 infusion pumps. The label revision is a re-wording meant to provide further context around need to inspect the fluid shield and the regulator closer to compliment the warnings that are currently part of the technical service manual.
Affected products
A) Plum A+ Volumetric Infusion Pump
Lot or serial number
All serial numbers.
Model or catalog number
12391
20679
20792
Companies
- Manufacturer
-
Hospira Inc.
275 North Field Drive
Lake Forest
60045
Illinois
UNITED STATES
B) Plum A+3 Infusion Pumps
Lot or serial number
All serial numbers.
Model or catalog number
12618
20678
Companies
- Manufacturer
-
Hospira Inc.
275 North Field Drive
Lake Forest
60045
Illinois
UNITED STATES