FDA Device recall Z-0144-2027
Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack (10 pk), Item Number 670272-KIT
- FDA Device
- Class II
- ongoing
- Published 2026-10-21
On 2026-10-21 the FDA classified a Class II recall of Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack (10 pk), Item Number 670272-KIT by Sarnova Hc, citing affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0144-2027 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-06-12 |
| Published | 2026-10-21 |
| Last updated | 2026-10-27 05:30 UTC |
| Company | Sarnova Hc |
| Distribution | US |
Product
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.
Identifiers
| code_info | Lot ASM0043314 UDI-DI 00810094576127 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-10-27 05:30 UTC. Current status: ongoing.
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FDA Device · Class II · 2024-03-27 · Sarnova Hc - Curaplex Field Cric Kit with ET Tube, Item Number 36611
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FDA Device · Class II · 2024-01-24 · Sarnova Hc
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0144-2027%22
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