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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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High RiskFDA Device
Medical Devices

Smiths Medical CADD-Solis Infusion Pump AC Adapters Recalled for Electric Shock

Agency Publication Date: November 15, 2024
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Summary

Smiths Medical ASD, Inc. has recalled approximately 156,400 AC adapters for CADD-Solis Li-ion Rechargeable Battery Packs used with CADD-Solis infusion pumps. The recall affects Model Number REF 21-0270-25, which can become damaged or broken during use. If the adapter plug is damaged, metal contacts may be exposed or the prongs may separate, posing a danger to users. No injuries have been reported in the provided data, and consumers should contact the manufacturer or their distributor for a replacement or repair.

Risk

The adapter's input plug can break, exposing live metal contacts or causing the electrical prongs to separate from the adapter body. This creates a significant risk of electric shock to healthcare providers or patients who touch the damaged components.

What You Should Do

  1. This recall involves the Smiths Medical CADD-Solis AC adapters (Model 21-0270-25) used with CADD-Solis Li-ion Rechargeable Battery Packs and infusion pumps. All lots with UDI/DI 15019517126844 are included in this recall.
  2. Stop using any AC adapter that shows signs of physical damage, such as cracks in the casing, exposed metal contacts, or loose/separated electrical prongs.
  3. Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.
  4. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) for additional information or questions regarding this recall.

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer correction/replacement program.

How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Smiths Medical CADD-Solis Li-ion Rechargeable Battery Packs AC adapter
Model / REF:
REF 21-0270-25
Lot Numbers:
All lots
UDI:
15019517126844

Used with CADD-Solis infusion pumps.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95483
Status: Active
Manufacturer: Smiths Medical ASD, Inc.
Sold By: medical distributors; specialty healthcare retailers
Manufactured In: United States
Units Affected: 156,400 AC adapters
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.