Biomet, Inc. recalls Vanguard 360 Revision System Posterior Augment With Bolt - P
Recalled Product
Vanguard 360 Revision System Posterior Augment With Bolt - Product Usage: intended for use in knee arthroplasty Item Number: 185422
Hazard / Issue
Incorrect bolt -tibial bolts in package instead of femoral bolts may delay procedure
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot Number: 098780 UDI Number: (01) 00880304482739 (17) 290501 (10) 098780
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