Smiths Medical recalls CADD Solis VIP Ambulatory Infusion Pumps with potential thermal damage. Affected models include 2120 series with specific serial numbers and UDI-DI codes. Contact for details.
There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP infusion pumps.
Smiths Medical is recalling certain CADD Solis VIP Ambulatory Infusion Pumps due to a potential for thermal damage. This could lead to burns or other injuries if the pump overheats. Affected units have specific model numbers and serial numbers listed in the recall notice.
The pumps may overheat due to a design flaw, potentially causing burns or other injuries. Thermal damage can occur if the pump is used for extended periods without proper cooling.
Patients using the CADD Solis VIP Ambulatory Infusion Pumps with model numbers 2120 and specific serial numbers are affected. Healthcare providers and patients who have these pumps at home or in medical facilities are most at risk.
Check the model number on the pump or kit, which is listed as 2120. Affected units have specific serial numbers and UDI-DI codes provided in the recall notice. The pumps are sold in the U.S. and other regions with English language support.
Look for the model number on the pump or kit, which should be 2120 for affected units.
Reach out to Smiths Medical for specific details about your pump and instructions on next steps.
The affected pumps have model numbers starting with 2120, such as 21-2127-0105-01, 21-2120-0105-01, and others listed in the recall notice.
Check the model number on the pump or kit. Affected units have specific serial numbers and UDI-DI codes provided in the recall notice.
The recall notice does not specify a fix or remedy; users are advised to contact Smiths Medical for details.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1682-2025 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-1682-2025 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.
