FDAFDA recall Z-0144-2027 · Oct 21, 2026
Sarnova HC, Llc: Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack (10 pk) recall
Recall found
Product
Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack (10 pk), Item Number 670272-KIT
Reason for recall
Affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- Lot ASM0043314 UDI-DI 00810094576127
- Quantity
- 2,500 kits
- Distribution
- US Nationwide distribution in the states of IA, IL, IN, KY, MI, MN, MO, ND, OH, UT.
- Recalling firm
- Sarnova HC, Llc, Dublin, OH
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-06-12
Source: openFDA enforcement record Z-0144-2027 · search recall number Z-0144-2027 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 26, 2026, 8:14 PM EDT. The agency notice is the final word.