FDAFebruary 27, 2024device

CADD-Solis Ambulatory Infusion Pumps, Model 2100. Intended for the following uses: Indicated for the following uses: Intra-arterial, subcutaneous, intraperitoneal, in close proximity to nerves, into an intraoperative site, epidural space or subarachnoid space. Therapies that require a continuous ...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

CADD-Solis Ambulatory Infusion Pumps, with software versions before v4.3, may have the following issues:1. Upstream Occlusion, 2. Stop and Power Keys Unresponsive, 3. Manual Mode Air Detector, 4. Single Bubble Air Detection, 5. Error Codes Not Displayed at Power Up, 6. Audible Alarm, 7. Low Sensitivity Air in Line Detection Threshold, 8. PharmGuard Server Password. Smiths Medical corrected many of the issues included in this notification in previous software updates and the corrections were carried forward into all subsequent software releases. Please ensure you have the most recent CADD software (v4.3 - 2023) installed on your pumps.

What to do

FDA enforcement status: Ongoing

Brands named

smiths medical asdsmithssmiths medical

UPCs

212101020002306105860353371061058603295021210101005010610586035548212101020003306105860353442121010200061061058603535721210102000730610586035368212101020012

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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