Health 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
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Products

Affected productsLot or serial numberModel or catalog number
CADD-Solis Ambulatory Infusion PumpMore 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

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