Smiths Medical recalls CADD Administration Sets (Model #21-7346-24) with potential incorrect air filter assembly. Affected units include specific lot numbers. Consumers should check their product details.
Product may have been manufactured with an air filter assembled in an incorrect orientation.
Smiths Medical is recalling CADD Administration Sets with model number 21-7346-24 due to a possible incorrect air filter assembly. This could affect the device's performance but does not pose an immediate safety risk.
The air filter may be assembled incorrectly, which could impact the device's function. This might lead to improper medication delivery but does not cause immediate injury or harm.
Healthcare professionals using these administration sets are likely affected. Patients receiving treatments through these devices may be at risk if the filter is not correctly assembled.
Check for model number 21-7346-24 on the device. Affected units have specific lot numbers: 3750848, 3776357, 3793886, 3766764, 3793887, 3796141, 3776356, 3793888, 3847669.
Identify the model number and lot numbers to confirm if your device is affected.
The recall is for potential incorrect air filter assembly, which may affect device function but does not pose an immediate safety risk.
Check the model number and lot numbers to see if your device is affected. If it is, contact Smiths Medical for further instructions.
Look for model number 21-7346-24 and check if your lot number is one of the listed numbers: 3750848, 3776357, 3793886, 3766764, 3793887, 3796141, 3776356, 3793888, 3847669.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0148-2022 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0148-2022 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.
