Health product recall

CADD Solis VIP Infusion Pump (2018-06-11)

Starting date:
June 11, 2018
Posting date:
June 29, 2018
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-67140

Affected products

CADD Solis VIP Infusion Pump

Reason

The purpose of this Field Safety Notice (FSN) is to inform you of concerns raised by Health Canada regarding delivery accuracy of the CADD Solis VIP Pump. This FSN clarifies the environmental factors and product configuration that may have an impact on delivery accuracy for the CADD Solis VIP Pump. This notification does not involve a retrieval of devices.

Affected products

CADD Solis VIP Infusion Pump

Lot or serial number

More than 1000 numbers, contact manufacturer.

Model or catalog number
  • 21-2120-0100-02
  • 21-2120-0100-50
  • 21-2120-0100-51
  • 21-2120-0100-95
  • 21-2120-0102 -02
  • 21-2120-0102-51
  • 21-2120-0102-78
  • 21-2120-0103-02
  • 21-2120-0103-51
  • 21-2120-0103-78
Companies
Manufacturer
Smiths Medical ASD, Inc.
1265 Grey Fox Road
St. Paul
55112
Minnesota
UNITED STATES