Health product recall

CADD-Solis™ Ambulatory Infusion Pump

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.

21-2101-0200-02
21-2111-0403-78
21-2112-0400-51
21-2112-0401-51
21-2112-0403-78
21-2102-51
21-2111-0100-51
21-2111-0300-00
21-2111-0400-51
21-2111-0401-51
21-2111-0403-51
21-2112-0200-02
21-2112-0300-50
21-2112-0403-02
21-2112-0403-51
21-2111-0300-02
21-2112-0300-02
21-2111-0300-50
21-2112-0100-51
21-2111-0403-02
21-2101-51
21-2111-0200-02

CADD-Solis VIP™ Ambulatory Infusion Pump

More than 10 numbers, contact manufacturer.

21-2120-0100-95
21-2120-0103-02
21-2120-0100-50
21-2120-0102-92
21-2120-0103-51
21-2120-0102-51
21-2120-0100-02
21-2120-0102 -02
21-2120-0102-78
21-2120-0103-78
21-2120-0100-51

Issue

Issue 1: Damage to the circuit board within the housing of the rechargeable battery pack  may cause melting of the plastic housing, specifically on the top and bottom surfaces. 

Issue 2: Damage to the wireless communication module circuit board may cause melting  of the plastic housing of the wireless communication module battery. 

Issue 3: Damaged or dislodged battery separators, or foreign material in the battery compartment, may cause an electrical short condition between the battery contacts.

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-77345

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