Medacta Usa Inc MectaLIF ANTERIOR - Antibackout Lag Cover, REF 03.30.305, interbody fusion device Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
MectaLIF ANTERIOR - Antibackout Lag Cover, REF 03.30.305, interbody fusion device
Brand
Medacta Usa Inc
Lot Codes / Batch Numbers
UDI/DI 07630345732330, All Lot Numbers
Products Sold
UDI/DI 07630345732330, All Lot Numbers
Medacta Usa Inc is recalling MectaLIF ANTERIOR - Antibackout Lag Cover, REF 03.30.305, interbody fusion device due to There is a potential for breakage of the small screw used to affix the anti-backout plate.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
There is a potential for breakage of the small screw used to affix the anti-backout plate.
Recommended Action
Per FDA guidance
Medacta USA initially notified its direct consignees by telephone on 03/08/2023 and followed with an URGENT - Field Safety Notice sent by email on 03/22/2023. The notice explained the issue and requested the units be returned and the notice be sent forward to all people and organizations potentially affected.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AZ, GA, ID, TX, VA
Page updated: Jan 10, 2026