Recall MonitorHealth Products
CADD-Solis™ Ambulatory Infusion Pump
· Published by Health Canada · Official notice
Details
Alert type: Health product recall
Category: Health products - Medical devices - General hospital and personal use
Product: CADD-Solis™ Ambulatory Infusion Pump
Issue: Medical devices - Performance
What to do: Contact the manufacturer if you require additional information.
Audience: Healthcare
Recall class: Type II
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