Home / Recalls / Medacta Usa Inc / Z-1402-2023

Z-1402-2023 Class II

Recalled by Medacta Usa Inc — Memphis, TN

Recall Details

Product Type
Devices
Report Date
April 26, 2023
Initiation Date
March 8, 2023
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
44 units

Product Description

MectaLIF ANTERIOR - Lag Plate Flush H14, REF 03.30.302, interbody fusion device

Reason for Recall

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

Distribution Pattern

US: ID, TX, GA, VA, AZ

Code Information

UDI/DI 07630345732309, All Lot Numbers

Other recalls by Medacta Usa Inc

  • Z-1401-2023 Class II — MectaLIF ANTERIOR - Lag Plate Flush H12, REF 03.30.301, interbody fusion device (March 8, 2023)
  • Z-1403-2023 Class II — MectaLIF ANTERIOR - Lag Plate Flush H16, REF 03.30.303, interbody fusion device (March 8, 2023)
  • Z-1404-2023 Class II — MectaLIF ANTERIOR - Lag Plate Flush H18, REF 03.30.304, interbody fusion device (March 8, 2023)
  • Z-1405-2023 Class II — MectaLIF ANTERIOR - Antibackout Lag Cover, REF 03.30.305, interbody fusion devic (March 8, 2023)
  • Z-1400-2023 Class II — MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device (March 8, 2023)
  • Z-0372-2023 Class II — NextAR Shoulder Surgical Technique, Shoulder NextAR RSA Platform, CT based compu (October 27, 2022)
  • Z-1247-2022 Class II — GMK Efficiency - GMK Sphere CR Insert Instrument Set Size 1 (April 13, 2022)
  • Z-0775-2020 Class II — Medacta Shoulder SYSTEM HUMERAL ANATOMICAL METAPHYSIS, REF 04.01.0023 through 04 (November 4, 2019)
  • Z-0196-2019 Class II — Medacta International MiniMAX CEMENTLESS ANATOMICAL STEM, 12/14: for cementless (November 15, 2017)
  • Z-0266-2018 Class II — The GMK knee system: designed for cemented use in total knee arthroplasty. Sphe (October 24, 2017)