Smiths Medical recalls CADD Administration Sets with specific list numbers and lot ranges due to potential underdelivery and 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 Administration Sets that may cause underdelivery of medication or false alarms indicating no disposable is attached. This could lead to incorrect dosing or treatment interruptions.
The sets may underdeliver medication due to tubing occlusion, causing incorrect dosing. They can also trigger false 'No Disposable Attached' alarms, leading to unnecessary treatment interruptions or confusion.
People using these specific CADD Administration Sets for medical infusion therapy are affected. Patients and caregivers who have the listed model numbers or lot ranges are most at risk.
Check for list numbers starting with REF 21-7300-24 through REF 21-7649-24 or the corresponding lot numbers and UDI/DI codes listed in the recall notice.
Look for the list numbers (REF codes) and lot numbers provided in the recall notice to confirm if your device is affected.
The recall includes CADD Administration Sets with list numbers from REF 21-7300-24 to REF 21-7649-24, along with specific lot numbers and UDI/DI codes.
The sets may cause underdelivery of medication due to tubing occlusion or trigger false 'No Disposable Attached' alarms, potentially leading to incorrect dosing or treatment interruptions.
No, but you should check if your device is affected and contact Smiths Medical if you have the listed model numbers or lot ranges.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0966-2023 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0966-2023 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.
