Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack recall (Sarnova HC, Llc)
Medical deviceClass IIOngoing
Summary: Sarnova HC, Llc is recalling Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack (10 pk), Item Number 670272-KIT. Reason: Affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula.
What is being recalled
Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack (10 pk), Item Number 670272-KIT
Why
Affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
US Nationwide distribution in the states of IA, IL, IN, KY, MI, MN, MO, ND, OH, UT. (states named: Iowa, Illinois, Indiana, Kentucky, Michigan, Minnesota, Missouri, North Dakota, Ohio, Utah)
How to tell if yours is affected
Lot ASM0043314 UDI-DI 00810094576127
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-0144-2027 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | June 12, 2026 |
| Reported | October 21, 2026 |
| Company | Sarnova HC, Llc |
| Company location | Dublin, OH, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 2,500 kits |
More recalls from Sarnova HC, Llc · all medical device recalls · recalls from June 2026