FDA recall Z-1400-2023

Product

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.

Distribution

US: ID, TX, GA, VA, AZ

Key facts

Status

Completed

Initiation date

2023-03-08

Report date

2023-04-26

Voluntary/Mandated

Voluntary: Firm initiated

Location

Memphis, TN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1400-2023