Smiths Medical recalls CADD-Solis Li-ion battery AC adapters (model REF 21-0270-25) due to potential plug damage causing exposed contacts or prong separation. All units are affected.
The adapter input plug can become damaged or broken. If the input plug is damaged, the metal contacts to the body of the AC adapter may be exposed or one or more of the AC mains prongs may separate from the input plug.
Smiths Medical is recalling its CADD-Solis Li-ion rechargeable battery AC adapters (model REF 21-0270-25) because the input plug can become damaged or broken. This could expose metal contacts or cause AC mains prongs to separate, creating a risk of electrical hazards.
The adapter's input plug can become damaged or broken over time. If damaged, metal contacts may become exposed or one or more AC mains prongs could separate from the plug, potentially causing electrical hazards.
Users of CADD-Solis infusion pumps who own the recalled AC adapter model REF 21-0270-25 are affected. Patients using these pumps with the recalled adapter face the highest risk.
Check for the model number REF 21-0270-25 on the adapter. The product is sold with CADD-Solis infusion pumps and has a unique identifier 15019517126844. All lots are affected.
Inspect the input plug for damage or broken contacts. If damaged, stop using the adapter immediately.
Yes, all units of model REF 21-0270-25 are affected.
If the input plug is damaged, stop using the adapter immediately and contact Smiths Medical for assistance.
Look for the model number REF 21-0270-25 on the adapter. The product is sold with CADD-Solis infusion pumps and has a unique identifier 15019517126844.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0466-2025 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0466-2025 from Smiths Medical. 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.
