MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device
Reported: April 26, 2023 Initiated: March 8, 2023 #Z-1400-2023
Product Description
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.
Details
- Recalling Firm
- Medacta Usa Inc
- Units Affected
- 32 units
- Distribution
- US: ID, TX, GA, VA, AZ
- Location
- Memphis, TN
Frequently Asked Questions
What product was recalled? ▼
MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device. Recalled by Medacta Usa Inc. Units affected: 32 units.
Why was this product recalled? ▼
There is a potential for breakage of the small screw used to affix the anti-backout plate.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 26, 2023. Severity: Moderate. Recall number: Z-1400-2023.
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