Product Wiki · Recalls · U.S. FDA — Device Enforcement

MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device — recall Z-1400-2023

U.S. FDA — Device Enforcement · United States · 2023-03-08 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1400-2023
Date of alert
2023-03-08
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medacta Usa Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
07630345732286
Reported risk: There is a potential for breakage of the small screw used to affix the anti-backout plate.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.