Sarnova recalls Curaplex Nasal Intubation Kits with 6mm Endotrol Tube due to incompatible endotracheal tube holder, risking airway management failure during nasal intubation.
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 6mm Endotrol Tube because the included endotracheal tube holder isn't compatible with nasal intubation procedures. This could leave medical professionals without the proper way to secure the tube during emergency airway management.
The endotracheal tube holder in certain kits doesn't work properly with nasal intubation. This means medical staff might not be able to securely fix the tube after insertion, potentially causing airway issues during emergency procedures.
Healthcare professionals using the recalled kits for nasal intubation procedures are most at risk. Patients undergoing emergency airway management with these kits could face complications.
Check for the item number 023060S or UDI/GTIN 00815277020008 (each) or 00810071639630 (case). The kits were sold with lot numbers ASM0038077, ASM0038129, ASM0038334, or ASM0038598.
Verify if the endotracheal tube holder works with your nasal intubation procedure by checking the product's compatibility documentation.
The endotracheal tube holder in certain kits is not compatible with nasal intubation procedures, leaving practitioners without the necessary means to secure the inserted tube.
Curaplex Nasal Intubation Kits with 6mm Endotrol Tube, item number 023060S, UDI/GTIN 00815277020008 (each) or 00810071639630 (case), with lot numbers ASM0038077, ASM0038129, ASM0038334, or ASM0038598.
The recall does not require immediate stop use; healthcare professionals should check compatibility before continuing use.
We’ve drafted a message you can send Sarnova to request your refund or repair — edit it as you like.
Subject: Recall Z-1307-2024 — Sarnova Sarnova Hello, I own a Sarnova that is covered by recall Z-1307-2024 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.
