RecallDepth

Curaplex Nasal Intubation Kit with 6mm Endotrol Tube-To perform a nasal intubation to establish an airway in an emergency. Item Number: 023060S

This recall is currently active, issued March 19, 2024. It was issued by Sarnova Hc, Llc.

Company
Sarnova Hc, Llc
Recall Initiated
February 12, 2024
Posted
March 19, 2024
Recall Number
Z-1307-2024
Quantity
540 kits
Firm Location
Dublin, OH
Official Source
View on FDA website ↗

Reason for Recall

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.

Distribution

US Nationwide distribution.

Lot / Code Info

UDI/GTIN: 00815277020008 each, 00810071639630 case Lot Numbers: ASM0038077 ASM0038129 ASM0038334 ASM0038598

Root Cause

Component design/selection

Action Taken

Bound Tree issued URGENT NOTICE OF RECALL letters on February 12, 2024 via USPS Letter to Medical Inventory Controls/Supplies Coordinator/Buyer. Letter states reason for recall, health risk and actin to take: Should you determine your inventory contains product covered by this recall, please immediately quarantine your affected product and contact Bound Tree Medical Customer Care at 800.533.0523 to arrange for a return of the product in exchange for a credit

More recalls by Sarnova Hc, Llc

View all recalls by this company →