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: 759.8 units Lot/code info: UDI-DI:00815686021207 Lot Number: 04617200805 and below
00815686021207, 04617200805
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.