Curaplex Capnography recallZ-0144-2027 · Sarnova HC, Llc · initiated Jun 12, 2026
Open, Classified All recalls posted in October 2026
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Sarnova HC, Llc or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula.
FDA root cause category: Nonconforming Material/Component
What the company is doing
Firm began notifying customers on June 12, 2026. Customers were instructed to inspect their kits from the affected lot to determine whether they contained the adult-sized cannula. If they found that the kit instead contained the pediatric cannula, customers were to discard the cannula and report it to the recalling firm. Bound Tree would then provide replacement adult nasal cannulas to the customer.
Recall details
- Recall number
- Z-0144-2027
- Recall class
- Not yet classified by the FDA
- Status
- Open, Classified
- Initiated by the company
- Jun 12, 2026
- Posted by the FDA
- Oct 9, 2026
- Recalling firm
- Sarnova HC, Llc
- Quantity
- 2,500 kits
- Product code
- CCX
- Distribution
- US Nationwide distribution in the states of IA, IL, IN, KY, MI, MN, MO, ND, OH, UT.
Product description
Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack (10 pk), Item Number 670272-KIT
Code information (models, lots, serial numbers)
Lot ASM0043314 UDI-DI 00810094576127
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- Curaplex® 670272-KITBound Tree Medical, LLC · ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE1 recall0 reports
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 18, 2026. Text above is shown as published by the FDA.
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