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Health product recall

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.