Sarnova recalls Curaplex Nasal Intubation Kits with 7mm endotracheal tubes due to incompatible tube holder affecting nasal intubation safety. Affected kits include specific lot numbers and item numbers.
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.
Sarnova is recalling Curaplex Nasal Intubation Kits with 7mm endotracheal tubes because the included tube holder isn't compatible with nasal intubation procedures. This could leave medical professionals without a way to secure the tube during emergency airway management.
The tube holder in certain kits doesn't work properly with nasal intubation, meaning medical staff might not be able to securely fix the endotracheal tube after insertion. This could lead to airway complications during emergency procedures.
Healthcare professionals using the recalled kits for emergency airway procedures are most at risk. Patients undergoing nasal intubation may be affected if the kit is used incorrectly.
Check for item number 023070S or UDI/GTIN 00815277020015 (each) or 00810071639647 (case). Affected kits have lot numbers ASM0038078, ASM0038130, ASM0038284, or ASM0038395.
Verify the item number, UDI/GTIN, and lot numbers listed in the recall notice to confirm if your kit is affected.
The tube holder in certain kits is not compatible with nasal intubation procedures, leaving medical staff without a way to secure the endotracheal tube.
Check the item number, UDI/GTIN, and lot numbers to see if your kit is affected. If it is, stop using it and contact Sarnova for further instructions.
The recall notice does not mention a fix or remedy; affected kits should be stopped from use.
We’ve drafted a message you can send Sarnova to request your refund or repair — edit it as you like.
Subject: Recall Z-1308-2024 — Sarnova Sarnova Hello, I own a Sarnova that is covered by recall Z-1308-2024 from Sarnova. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
