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Health product recall

Alaris PC Unit Model 8015. Software v9.17 and 9.19 (2016-06-06)

Starting date:
June 6, 2016
Posting date:
June 16, 2016
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
Healthcare Professionals, General Public, Hospitals
Identification number:
RA-58924

Affected products

  1. Alaris PC Unit Model 8015. Software v9.17 and 9.19

Reason

Software error will cause device to over or under dose patient. This error occurs if operator uses the restore feature under certain circumstances

Affected products

A. Alaris PC Unit Model 8015. Software v9.17 and 9.19

Lot or serial number

More than 100 numbers, contact manufacturer.  

Model or catalog number
  • 8015
Companies
Manufacturer
Carefusion 303, Inc.
10020 Pacific Mesa Blvd.
San Diego
92121-2733
California
UNITED STATES