Medacta Usa Inc: Medical Device Recall in 2023 - (Recall #: Z-1400-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device

Product Classification:

Class II

Date Initiated: March 8, 2023

Date Posted: April 26, 2023

Recall Number: Z-1400-2023

Event ID: 91947

Reason for Recall:

There is a potential for breakage of the small screw used to affix the anti-backout plate.

Status: Completed

Product Quantity: 32 units

Code Information:

UDI/DI 07630345732286, All Lot Numbers

Distribution Pattern:

US: ID, TX, GA, VA, AZ

Voluntary or Mandated:

Voluntary: Firm initiated