Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices
Reason for recall: Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices Distribution: Nationwide Quantity: 200 units Lot/code info: UDI-DI 00196449015993; Lot numbers 265814, 24060DF02, 24065DF03, 24060DF01. 24065DF05, 263512
00196449015993
Official record: FDA (Device enforcement) ↗
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