MectaLIF ANTERIOR - Lag Plate Flush H12 recall
MectaLIF ANTERIOR - Lag Plate Flush H12, REF 03.30.301, interbody fusion device
Why was MectaLIF ANTERIOR - Lag Plate Flush H12 recalled?
There is a potential for breakage of the small screw used to affix the anti-backout plate.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI/DI 07630345732293, All Lot Numbers
- Product
- MectaLIF ANTERIOR - Lag Plate Flush H12, REF 03.30.301, interbody fusion device
- Recalling firm
- Medacta Usa Inc
- Quantity
- 53 units
- Distribution
- US: ID, TX, GA, VA, AZ
- Recall date
- April 26, 2023
- Classification
- Class II
- Status
- Completed
- Agency
- FDA (device)