Medacta recalls MectaLIF Anterior Lag Plate Flush H14 (REF 03.30.3:02) interbody fusion devices due to potential screw breakage. All units with UDI/DI 07630345732309 are affected.
There is a potential for breakage of the small screw used to affix the anti-backout plate.
Medacta is recalling a specific type of spinal fusion device that could break, potentially causing complications. This recall affects all units with the unique identifier 07630345732309.
The small screw that holds the anti-backout plate in place could break during use, which might lead to device displacement or complications in spinal fusion.
Patients who received the MectaLIF Anterior Lag Plate Flush H14 (REF 03.30.302) interbody fusion device with UDI/DI 07630345732309 are affected. Spinal surgery patients are most at risk.
Check for the product name 'MectaLIF Anterior Lag Plate Flush H14' with reference number 03.30.302. All units with the unique identifier 07630345732309 are affected.
Identify if your device has the unique identifier 07630345732309.
The recall indicates a potential for screw breakage, but the risk is low and does not cause serious injury in normal use.
Check for the product name 'MectaLIF Anterior Lag Plate Flush H14' with reference number 03.30.302 and unique identifier 07630345732309.
The recall does not specify a remedy, so contact Medacta for further instructions.
We’ve drafted a message you can send Medacta to request your refund or repair — edit it as you like.
Subject: Recall Z-1402-2023 — Medacta Medacta Hello, I own a Medacta that is covered by recall Z-1402-2023 from Medacta. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
