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Plum A+ Single Channel Infusers
- Starting date:
- October 30, 2012
- Posting date:
- December 10, 2012
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public (GP), Healthcare Professionals, Hospitals
- Identification number:
- RA-16327
Recalled Products
- Plum A+ Single Channel Infusers - V. Knob
- Plum A+ Single Channel Infusers - V. Knob
- Plum A+ Single Channel Infusers - V. Knob
Reason
Certain Plum A+ Family Infusion pumps in which the audio level rotary knob does not rotate in accordance with the information in the systems operating manual (SOM). The SOM indicates a clockwise rotation of the knob will decrease the alarm volume, however in some Plum A+ devices, it has been found that the volume increases when the knob is turned clockwise.
Affected products
A. Plum A+ Single Channel Infusers - V. Knob
Lot or serial number
All Serial Numbers
Model or catalog number
12097, 12391, 20679, 20791, 20792
Companies
- Manufacturer
- Hospira Inc.
B. Plum A+ Single Channel Infusers - V. Knob
Lot or serial number
All Serial Numbers
Model or catalog number
20677
Companies
- Manufacturer
- Hospira Inc.
C. Plum A+ Single Channel Infusers - V. Knob
Lot or serial number
All Serial Numbers
Model or catalog number
11005, 11006
Companies
- Manufacturer
- Hospira Inc.