Trackx Technology Inc FDA Recalls

2 recalls on file across devices, 0 of them Class I and 1 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
Product Name: Insight Base Flex - 8, Ref 608-3TX; The device consists of a sterile Snap that includes reflective featureClass IIISep 3, 2024The patient label stickers may have the wrong expiration dat	The patient label stickers may have the wrong expiration date recorded. The contract manufacturer entered the	Class IIIDevices	Sep 3, 2024
TrackX Insight Base Modular Instrument Tracker, 5L, REF #604-3TX, Sterile; and TrackX Insight Base Modular Instrument TClass IIOct 24, 2022The device is breaking and falling off the Nuvasive T-Handle	The device is breaking and falling off the Nuvasive T-Handle with Hudson Adapter on certain Nuvasive XLIF inst	Class IIDevices	Oct 24, 2022