MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device
FDA Recall #Z-1400-2023 — Class II — March 8, 2023
Product Description
MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device
Reason for Recall
There is a potential for breakage of the small screw used to affix the anti-backout plate.
Recalling Firm
Medacta Usa Inc — Memphis, TN
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Devices
Product Quantity
32 units
Distribution
US: ID, TX, GA, VA, AZ
Code Information
UDI/DI 07630345732286, All Lot Numbers
Status
Completed
Voluntary / Mandated
Voluntary: Firm initiated