Smiths Medical recalls CADD Administration Sets with specific list numbers and lot ranges due to potential underdelivery and false 'No Disposable Attached' alarms. Affected users 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 several CADD Administration Sets that may cause underdelivery of medication or false alarms indicating no disposable is attached. This could lead to incorrect dosing or missed treatments.
The sets may underdeliver medication due to tubing occlusion, causing incorrect dosing. They can also trigger false 'No Disposable Attached' alarms, leading to unnecessary interruptions in treatment.
Patients using the recalled CADD Administration Sets for medical infusion therapy are most at risk. Healthcare providers and patients with specific lot numbers or list numbers should check if their device is affected.
Check for list numbers like REF 21-7300-24 through REF 21-7395-24 or lot numbers from 3630772 through 4339178 on the device packaging or label.
Review the list numbers and lot numbers on the device packaging to confirm if it is affected.
The recalled sets include list numbers REF 21-7300-24 through REF 21-7395-24.
Check the list numbers and lot numbers on the device packaging; affected units have specific ranges listed in the recall notice.
The recall does not specify a remedy, so contact Smiths Medical directly for guidance on next steps.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0963-2023 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0963-2023 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.
