Smiths Medical ASD, Inc. is a leading manufacturer of medical devices and equipment. Explore our comprehensive product catalog for healthcare professionals.
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.
Smiths Medical ASD, Inc. is a leading manufacturer of medical devices and equipment. Explore our comprehensive product catalog for healthcare professionals.
Low risk of harm due to standard medical device safety protocols
Healthcare professionals
Check for proper certification and compliance with medical device regulations
Verify the manufacturer's credentials and certifications
Ensure the product meets relevant medical device standards
Consult with healthcare professionals for specific use cases
Smiths Medical ASD, Inc. is a leading manufacturer of medical devices and equipment for healthcare professionals.
Yes, Smiths Medical ASD, Inc. products are certified and meet international medical device standards.
Ensure the product meets relevant medical device regulations and standards, and consult with healthcare professionals for specific use cases.
We’ve drafted a message you can send Smiths Medical ASD, Inc. to request your refund or repair — edit it as you like.
Subject: Recall Z-2419-2024 — Smiths Medical ASD, Inc. Smiths Medical ASD, Inc. Hello, I own a Smiths Medical ASD, Inc. that is covered by recall Z-2419-2024 from Smiths Medical ASD, Inc.. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
