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Alaris Pump Module Model 8100 – Pump Module Door Keypad Overlay
- Starting date:
- July 27, 2012
- Posting date:
- September 3, 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, Healthcare Professionals, Hospitals
- Identification number:
- RA-23835
Recalled Products
A. Alaris Pump Module Model 8100
Reason
A potential risk has been identified with the Alaris Pump Module Model 8100. The Pump Module Door Keypad Overlay can potentially separate from underlying assembly which could lead to fluid ingressess. Cleaning a separated keypad or fluid spill can lead to a fluid ingress.
Affected products
A. Alaris Pump Module Model 8100
Lot or serial number
More than 10 numbers, contact manufacturer
Model or catalog number
8100LVP
Companies
- Manufacturer
- Carefusion 303, Inc.