Sarnova HC Recalls Curaplex Capnography Cannula Multipacks Due to Pediatric Cannula Risk
Sarnova HC recalls 2,500 Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipacks (10 pk) with pediatric nasal cannulas instead of adult ones. Affected kits were sold nationwide in 2026.
Use caution until it’s fixed
Affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula.
What happened, in plain English
Sarnova HC recalls 2,500 Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipacks (10 packs) because they were assembled with pediatric nasal cannulas instead of adult ones. This could cause improper use in adult patients needing medical monitoring. Read more at govinfonow.com/recall/1765338-sarnova-hc-llc-recalls-curaplex-capnography-etco2-o2-oral-nasal.
Source Summary by GovInfoNow · govinfonow.com/recall/1765338-sarnova-hc-llc-recalls-curaplex-capnography-etco2-o2-oral-nasal · Updated October 27, 2026 · FDA enforcement record: FDA #Z-0144-2027
Cite this page
“Sarnova HC Recalls Curaplex Capnography Cannula Multipacks Due to Pediatric Cannula Risk.” GovInfoNow, updated October 27, 2026. https://govinfonow.com/recall/1765338-sarnova-hc-llc-recalls-curaplex-capnography-etco2-o2-oral-nasal. Based on FDA recall #Z-0144-2027 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0144-2027%22&limit=1).
Why it’s dangerous
The kits were assembled with pediatric nasal cannulas instead of adult ones. This could lead to improper oxygen delivery or inadequate monitoring during medical procedures.
Who’s affected
Adult patients using medical capnography equipment are most at risk. Healthcare providers who purchased the affected kits may also be affected.
How to tell if you have this one
Check for the item number 670272-KIT and lot number ASM0043314 on the packaging. The kits were sold nationwide in the U.S. starting in 2026.
- Brand
Sarnova HC- Category
Medical device
What to do — step by step
Check Kit Details
Look for item number 670272-KIT and lot number ASM0043314 on the packaging.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 10 states.
FDA distribution: “US Nationwide distribution in the states of IA, IL, IN, KY, MI, MN, MO, ND, OH, UT.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Illinois, Indiana, Iowa, Kentucky, Michigan, Minnesota, Missouri, North Dakota, Ohio, Utah.
Recall timeline
FDA published this recall 4 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-0144-2027 (June 12, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0144-2027 to see it in context.
- Plain-language summary written by qwen3:4b on October 27, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.