Smiths Medical recalls CADD infusion sets with specific model numbers and lot ranges due to potential underdelivery of medication or false 'No Disposable Attached' alarms. Consumers should check their product details.
There are two potential issues with CADD Infusion System Infusion Sets: (1) Lack of Delivery or Underdelivery related to Tubing Occlusion and (2) False "No Disposable Attached (NDA)" Alarms
Smiths Medical is recalling certain CADD infusion sets that may underdeliver medication or trigger false alarms about missing disposables. This could lead to incorrect dosing or treatment interruptions.
The infusion sets may have tubing that gets blocked, causing medication to not be delivered properly. They might also give false alarms indicating no disposable component is attached when it actually is.
Patients using these specific CADD infusion sets for medication delivery are affected. Those with the listed model numbers and lot ranges are most at risk.
Check for model numbers REF 21-7600-24, REF 21-7609-24, REF 21-7624-24, or REF 21-7649-24 with specific lot numbers listed in the recall notice.
Identify your model number and lot numbers to confirm if your CADD infusion set is affected.
Model numbers REF 21-7600-24, REF 21-7609-24, REF 21-7624-24, and REF 21-7649-24 with specific lot ranges.
The recall is due to potential underdelivery of medication or false alarms about missing disposable components.
The recall does not require immediate stoppage; however, you should check your product details to confirm if affected.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0965-2023 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0965-2023 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.
