Smiths Medical recalls CADD-Solis infusion pumps with potential thermal damage. Affected models include various versions of CADD-Solis Model 2110 and 2100 pumps with specific serial numbers. Contact for details.
There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP infusion pumps.
Smiths Medical is recalling several versions of CADD-Solis infusion pumps due to a potential risk of thermal damage. This could cause burns or other injuries if the pump overheats. Affected units have specific model numbers and serial numbers listed in the recall.
The pumps may overheat due to a design flaw, potentially causing burns or other injuries to users. Thermal damage can occur if the pump is left running for extended periods without proper cooling.
Patients using these infusion pumps for medical treatments are most at risk. Healthcare providers who use the pumps in clinical settings may also be affected.
Check for model numbers 2100 or 2110 with specific serial numbers listed in the recall. The pumps are labeled as CADD-Solis and may have yellow keypads or be trial/loaner units.
Look for the model number on the pump, which is listed as 2100 or 2110 with specific serial numbers provided in the recall.
Reach out to Smiths Medical for assistance with identifying and replacing affected units using the provided serial numbers.
No, only specific models with the listed serial numbers are affected. Check the model number and serial number against the recall list.
Look for the model number 2100 or 2110 with the specific serial numbers listed in the recall. The pumps may have yellow keypads or be trial/loaner units.
The recall does not require immediate discontinuation; however, you should check if your pump is affected and contact Smiths Medical for guidance.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1681-2025 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-1681-2025 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.
