ClearanceBrief
Recall Z-1884-2020 ยท FFK Lithotriptor, Electro-Hydraulic

Northgate Technologies, Inc.

AUTOLITH URO-TCH 9FR PROBE 54CM; NTI Catalog Number 9-203-0543 - Product Usage: Probes are used for the fragmentation of urinary/renal and biliary calculi.

DateMar 24, 2020 (initiated Mar 10, 2020)
StatusTerminated
ReasonInvestigation into a biocompatibility test discrepancy where a lot failed biocompatibility testing.
Root causeNonconforming Material/Component
ActionNorthgate Technologies, Inc. notified customers on 03/11/2020 via "Urgent: medical Device Recall Notification" email. The recall notice identified the affected and requested the customers to cease distribution and destroy affected product. The customers were asked to complete the "Recall Acknowledgment Form".
Quantity198 boxes. 3 units per box.
DistributionUS Nationwide distribution. No governmental.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K130368AUTOLITH TOUCH; URO TOUCH
Northgate Technologies, Inc., Nov 15, 2013