FDAFDA · Food and drugs·Recall number Z-1400-2023
MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device
Published April 26, 2023 · Recall initiated: March 8, 2023
Status when published: Completed — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
There is a potential for breakage of the small screw used to affix the anti-backout plate.
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Manufacturer
- Medacta Usa Inc
- Distributor
- US: ID, TX, GA, VA, AZ
- Lot
- UDI/DI 07630345732286, All Lot Numbers
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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