Recall archive / FDA device enforcement
MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device — FDA record Z-1400-2023
Reported completed
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Mar 8, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device
- Reason
- There is a potential for breakage of the small screw used to affix the anti-backout plate.
- Classification
- Class II
- Recalling firm
- Medacta Usa Inc
- Quantity
- 32 units
- Agency-reported status
- Completed
- Source record identifier
- Z-1400-2023
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | UDI/DI 07630345732286, All Lot Numbers |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US: ID, TX, GA, VA, AZ
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Apr 26, 2023
- Recall initiation date
- Mar 8, 2023
- Center classification date
- Apr 19, 2023
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.