Electromagnetic (EM) sensor tracking malfunction impacts the use of navigation functionality during endobronchial procedures and prompts the system to report a coil break warning message. This could result in a potential procedural delay
Reason for recall: Electromagnetic (EM) sensor tracking malfunction impacts the use of navigation functionality during endobronchial procedures and prompts the system to report a coil break warning message. This could result in a potential procedural delay Distribution: Worldwide Distribution: US (Nationwide) and OUS (foreign) to countries of: CN, DE, HK, IT, KR, SG, TH & TW. Quantity: 254.4 units Lot/code info: UDI-DI: 00815686020552 Lot Numbers: 05010210512 and below
00815686020552, 05010210512
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.