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Plum A+/A+3 Infuser Family of Infusers
- Starting date:
- December 10, 2012
- Posting date:
- January 7, 2013
- 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-16627
Recalled Products
- Plum A+ Volumetric Infusion Pump
- Plum A+3 Infusion Pump
Reason
The door roller assembly on the Plum A+/A+3 infuser family of infusers has the potential to break which can lead to possible unrestricted flow and/or overdelivery during the removal of the IV administration set's cassette from the pump.
Affected products
A. Plum A+ Volumetric Infusion Pump
Lot or serial number
All Serial Numbers
Model or catalog number
1231, 20679, 20792
Companies
- Manufacturer
- Hospira Inc.
B. Plum A+3 Infusion Pump
Lot or serial number
All Serial Numbers
Model or catalog number
1268, 20678
Companies
- Manufacturer
- Hospira Inc.