Smiths Medical recalls two CADD infusion sets due to potential underdelivery or false "No Disposable Attached" alarms. Affected units have specific list numbers and lot ranges.
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 two types of CADD infusion sets because they may cause underdelivery of medication or false alarms indicating no disposable is attached. This could lead to incorrect dosing or treatment delays.
The infusion sets may have tubing that gets blocked, causing medication to not deliver properly. They may also trigger false alarms that indicate no disposable is attached, even when it is.
Healthcare professionals using the CADD infusion sets for medication administration are most at risk. Patients receiving treatment through these sets could experience incorrect dosing or treatment delays.
Check the list numbers: REF 21-7346-24 or REF 21-7363-24. Lot numbers for REF 21-7346-24 range from 3776356 to 4320785, and for REF 21-7363-24 range from 3773412 to 4334343.
If the system shows a "No Disposable Attached" alarm when a disposable is present, stop using the set immediately.
If medication delivery seems slow or inconsistent, stop using the set and contact Smiths Medical for assistance.
The recalled sets have list numbers REF 21-7346-24 and REF 21-7363-24.
For REF 21-7346-24, lot numbers range from 3776356 to 4320785. For REF 21-7363-24, lot numbers range from 3773412 to 4334343.
Check the list number and lot number on your set against the ranges 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-0962-2023 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0962-2023 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.
