Reported Mar 27, 2024 · Ongoing
Curaplex Nasal Intubation Kit with 6mm Endotrol Tube-To perform a nasal intubation to establish an airway in an…
Sarnova HC, LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Sarnova HC, Llc · 5000 Tuttle Crossing Blvd · Dublin, OH · 43016-1534
Is this the product you have?
- Curaplex Nasal Intubation Kit with 6mm Endotrol Tube-To perform a nasal intubation to establish an airway in an emergency
- Item Number023060S
- Lot codes and dates
- UDI/GTIN
00815277020008 each00810071639630
- case Lot NumbersASM0038077 ASM0038129 ASM0038334 ASM0038598
- UDI/GTIN
- Amount recalled
- 540 kits
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
Endotracheal Tube Holder included in certain kits is not compatible with a nasal intubation procedure, leaving practitioners without the necessary means to secure the inserted endotracheal tube.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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