Sarnova Curaplex Capnography Oral Nasal Cannula Multipack
The Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack contains pediatric nasal cannulas instead of adult ones.
Moderate risk
Using it may cause temporary or medically reversible health problems. Serious harm is unlikely.
FDA Class II recall · How risk is rated
What happened
Sarnova HC, Llc is recalling 2,500 kits of the Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack (10 pk), Item Number 670272-KIT, because the affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula. The company began the recall on June 12, 2026, and the FDA added it to the Enforcement Report and classified it on October 9, 2026.
Summary by Recall Canary from the FDA notice.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is your kit affected?
Match the UDI-DI or item number and lot code listed under your product.
Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack (10 pk), Item Number 670272-KIT
- UDI-DI
- 00810094576127
- Lot
- ASM0043314
- Item
- 670272-KIT
Details
- Company began the recall
- Event ID
- 99838
- Company
- Sarnova HC, Llc
- Hazard
- Device defect
- Quantity recalled
- 2,500 kits
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
