Health product recall

CADD-Solis Ambulatory Infusion Pump

Brand(s)
Smiths Medical Asd Inc.
Last updated

Summary

Product
CADD-Solis Ambulatory Infusion Pump
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

CADD-Solis Ambulatory Infusion Pump

More than 10 numbers, contact manufacturer.

21-2101-0100-95
21-2101-0200-00
21-2101-0200-02
21-2111-0400-78
21-2111-0403-78
21-2112-0200-51
21-2112-0400-51
21-2112-0401-51
21-2112-0403-78
21-2101-0200-232
21-2102-0200-249
21-2111-0200-249
21-2112-0100-00
21-2112-0400-249
21-2101-0200-95
21-2102-51
21-2111-0100-51
21-2111-0300-95
21-2111-0401-78
21-2111-0403-92
21-2112-0300-95
21-2112-0401-78
21-2112-0403-92
21-2101-0200-249
21-2102-0200-95
21-2111-0300-00
21-2111-0400-51
21-2111-0401-51
21-2111-0403-51
21-2112-0200-02
21-2112-0300-50
21-2112-0400-78
21-2112-0403-02
21-2112-0403-51
21-2111-0200-232
21-2111-0300-02
21-2111-0400-249
21-2112-0200-00
21-2112-0200-95
21-2112-0300-02
21-2102-0200-00
21-2111-0300-50
21-2111-0400-01
21-2112-0100-51
21-2111-0100-249
2110

Issue

CADD-Solis pumps may lose communication with the CADD wireless communication module if wireless network setting changes on the hospital network are not compatible with the CADD wireless communication module. This may result in a "wireless module intermittent connection" high priority alarm, which will stop an ongoing infusion.

Recall Start Date: April 8, 2025

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies

Smiths Medical Asd, Inc.

6000 Nathan Lane N., Minneapolis, Minnesota, United States, 55442

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-77321

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