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Health product recall

ALARIS SYSTEM- SYRINGE PUMP MODULE MODEL 8110 SOFTWARE VERSIONS 9.15 AND 10.5

Starting date:
August 12, 2016
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-60054

Affected Products

ALARIS SYSTEM- SYRINGE PUMP MODULE MODEL 8110 SOFTWARE VERSIONS 9.15 AND 10.5

Reason

CAREFUSION HAS IDENTIFIED AN ISSUE WITH THE ALARIS SYRINGE PUMP MODULE 8110 SOFTWARE VERSIONS 9.15 AND 10.5.  INFUSION CAN UNEXPECTEDLY STOP WHEN AN INFUSION IS TRANSITIONING FROM ONE STATE TO ANOTHER.

Affected products

ALARIS SYSTEM- SYRINGE PUMP MODULE MODEL 8110 SOFTWARE VERSIONS 9.15 AND 10.5

Lot or serial number

More than 10 lots, contact manufacturer.
 

Model or catalog number

8110

Companies
Manufacturer
Carefusion 303, Inc.
10020 Pacific Mesa Blvd.
San Diego
92121-2733
UNITED STATES