Public recall detail

CADD-Solis Ambulatory Infusion Pump

2025-04-23

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Recall Safety notice
Quick summary

Quick summary: CADD-Solis Ambulatory Infusion Pump. Date: 2025-04-23.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: CADD-Solis Ambulatory Infusion Pump. Date: 2025-04-23.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandSmiths Medical Asd Inc.
ProductCADD-Solis Ambulatory Infusion Pump
IssueMedical devices - Performance
Recall classType II
IdentificationRA-77321

Affected products

ProductCADD-Solis Ambulatory Infusion Pump
LotMore than 10 numbers, contact manufacturer.
Model21-2101-0100-95 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
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionCADD-Solis Ambulatory Infusion Pump

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

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - General hospital and personal use
CompaniesSmiths Medical Asd, Inc. 6000 Nathan Lane N., Minneapolis, Minnesota, United States, 55442
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-77321
Background{}
CompaniesSmiths Medical Asd, Inc. 6000 Nathan Lane N., Minneapolis, Minnesota, United States, 55442
AudiencesHealthcare
Source updated2025-04-23

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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