Smiths Medical recalls certain Nasopharyngeal Airway sizes due to potential uncertainty in sterile packaging seal integrity. Affected units include specific model numbers and lot numbers listed in the recall notice.
Uncertainty in the seal integrity of the sterile packaging.
Smiths Medical is recalling specific sizes of Nasopharyngeal Airways because the sterile packaging might not seal properly. This could lead to contamination or infection if the product is used without proper sterility.
The sterile packaging may not seal correctly, potentially allowing contamination or infection if the airway is used without proper sterility. This is a concern for medical procedures where sterility is critical.
Healthcare professionals and patients using these airways for medical procedures. Those with the specific model numbers and lot numbers listed in the recall are most at risk.
Check the product label for the model size (6.0mm, 7.0mm, or 8.0mm) and the reference code (e.g., 100/210/060, 100/210/060JP). Also, verify the lot numbers and UDI/DI codes listed in the recall notice.
Look for the model size (6.0mm, 7.0mm, or 8.0mm) and reference code (e.g., 100/210/060) on the packaging.
Compare the lot numbers and UDI/DI codes on your product with the list provided in the recall notice.
Smiths Medical recalls Nasopharyngeal Airways with sizes 6.0mm, 7.0mm, and 8.0mm, including specific reference codes like 100/210/060 and lot numbers listed in the recall notice.
Check the product label for the model size and reference code, then compare the lot numbers and UDI/DI codes with the list provided in the recall notice.
The recall notice does not specify a remedy, so contact Smiths Medical directly for further instructions.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0143-2025 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0143-2025 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.
