Smiths Medical recalls CADD-Legacy 1 Model 6400 infusion pumps with non-matching serial numbers. Affected units may have incorrect serial numbers listed on the pump label versus software. No action is required for these units.
Certain CADD Legacy 1, Ambulatory Infusion Pumps, may contain non-matching serial numbers. The label attached to the back of the pump may list a serial number that does not match the correct serial number programmed into the software of the pump.
Smiths Medical is recalling certain CADD-Legacy 1 Model 6400 Ambulatory Infusion Pumps that have non-matching serial numbers between the pump label and its software. This issue does not cause immediate harm but requires verification to ensure safe use.
The pump's label may show a serial number that does not match the one programmed into its software. This mismatch could lead to incorrect dosing or malfunction if the pump is used without proper verification.
Patients using these specific infusion pumps for medical treatment. Those with the listed serial numbers are most at risk if they do not verify the pump's serial number matches the software.
Check the serial number on the pump's back label. Affected pumps have serial numbers from 409963 to 410020. These units were sold with the model number CADD-Legacy 1, Model 6400, REF 21-6400-51.
Look for the serial number on the back of the pump and compare it to the list of affected serial numbers (409963 to 410020).
No action is required for these pumps. The recall is for verification only; the pumps are safe to use if the serial number matches the software.
The affected pumps have serial numbers from 409963 to 410020.
This issue does not cause immediate harm. The pump is safe to use if the serial number matches the software.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0307-2018 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0307-2018 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.
