Smiths Medical recalls CADD Administration Sets with specific list numbers due to potential underdelivery and false 'No Disposable Attached' alarms. Affected units include certain lot numbers and model variants.
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 specific 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 insufficient doses. They also trigger false 'No Disposable Attached' alarms, which could lead to treatment interruptions or incorrect dosing.
Healthcare providers using the recalled CADD Administration Sets for medication delivery are most at risk. Patients receiving treatments through these sets could experience treatment errors.
Check for list numbers REF 21-7308-24, REF 21-7309-24, REF 21-7310-24, or REF 21-7308-24JP/REF 21-7309-24JP. Affected units have specific lot numbers ranging from 4053922 to 4334076 or similar ranges.
Identify if your CADD Administration Set has list numbers REF 21-7308-24, REF 21-7309-24, REF 21-7310-24, or REF 21-7308-24JP/REF 21-7309-24JP.
Check if your set's lot numbers fall within the ranges provided: 4053922-4334076 for REF 21-7308-24, 4062405-4334085 for REF 21-7309-24, or 4062404-4330874 for REF 21-7310-24.
The sets may underdeliver medication due to tubing occlusion or trigger false 'No Disposable Attached' alarms, which could lead to incorrect dosing or treatment interruptions.
Check for list numbers REF 21-7308-24, REF 21-7309-24, REF 21-7310-24, or REF 21-7308-24JP/REF 21-7309-24JP, and verify if your lot numbers fall within the specified ranges.
No, but you should check if your set is affected and take action if it is, as the hazard requires caution rather than immediate discontinuation.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0964-2023 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0964-2023 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.
