Capnia recalls Precision Sampling Set REF C20206 for use with CoSense ETCO monitors due to potential higher carbon monoxide readings during clinical tests. Affected units sold with specific lot numbers.
Sampling set nasal cannula used with End-Tidal Carbon Monoxide (ETCO) monitor may have residual carbon monoxide and volatile organic compounds present due to insufficient aeration of the cannula's carbon filter prior to sealing, which may lead to higher than expected ETOCc scores during clinical evaluations.
Capnia is recalling its Precision Sampling Set (REF C202:20206) for use with CoSense End-Tidal Carbon Monoxide monitors. The recall is because the nasal cannula may have higher carbon monoxide readings during clinical tests due to insufficient aeration of the carbon filter.
The sampling set's nasal cannula may not aerate properly before sealing, leading to residual carbon monoxide and volatile organic compounds. This can cause higher than expected carbon monoxide scores during clinical evaluations.
Healthcare professionals using the Precision Sampling Set with CoSense monitors are most at risk. The recall affects units sold with specific lot numbers and serial codes.
Check for the product name 'Precision Sampling Set' with reference number C20206. Affected units were sold with lot number 231220 and serial code 00858481006017.
Look for the reference number C20206 and lot number 231220 on the product packaging.
The nasal cannula may have residual carbon monoxide and volatile organic compounds due to insufficient aeration of the carbon filter before sealing, which can lead to higher than expected carbon monoxide scores during clinical evaluations.
Check for the reference number C20206 and lot number 231220 on the product packaging. Affected units were sold with serial code 00858481006017.
The recall record does not specify a remedy, so check with Capnia Inc for further instructions.
We’ve drafted a message you can send Capnia to request your refund or repair — edit it as you like.
Subject: Recall Z-2198-2025 — Capnia Capnia Hello, I own a Capnia that is covered by recall Z-2198-2025 from Capnia. 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.
