Smiths Medical recalls CADD-Solis VIP Ambulatory Infusion Pumps with specific model numbers due to risk of false upstream occlusion alarms interrupting therapy, potentially causing serious injury or death.
Affected pumps may trigger an erroneous (false) Upstream Occlusion Alarm under certain conditions, which will interrupt an active infusion. Interruption or delay of therapy can lead to serious patient injury or death.
Smiths Medical is recalling certain CADD-Solis VIP Ambulatory Infusion Pumps that may trigger false alarms, which can interrupt critical medication delivery and lead to serious injury or death. Affected units have specific model numbers listed in the recall.
The pumps may trigger a false 'upstream occlusion' alarm under certain conditions, which can interrupt active medication delivery. This interruption or delay in therapy could lead to serious injury or death for patients who rely on the pump.
Patients using the recalled pumps for medical infusion therapy are most at risk. The recall affects individuals with specific model numbers listed in the notice.
Check your pump's model number against the list of affected serial numbers provided in the recall notice. The affected models include specific combinations like 21-2120-0100-02 through 21-2127-0105-50L.
Identify your pump's model number and compare it to the list of affected serial numbers provided in the recall notice.
No, but you should check your model number against the list of affected units to determine if your pump is recalled. The recall does not require immediate discontinuation but requires verification.
The recall does not specify a remedy, so you should contact Smiths Medical directly for guidance on next steps if your pump is affected.
Check your pump's model number against the list of affected serial numbers provided in the recall notice.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1668-2025 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-1668-2025 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.
