CADD-Solis™ Ambulatory Infusion Pump
Brand(s)
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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