Biomet, Inc.: Medical Device Recall in 2020 - (Recall #: Z-0723-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Vanguard 360 Revision System Posterior Augment With Bolt - Product Usage: intended for use in knee arthroplasty Item Number: 185422

Product Classification:

Class II

Date Initiated: December 1, 2020

Date Posted: December 30, 2020

Recall Number: Z-0723-2021

Event ID: 86923

Reason for Recall:

Incorrect bolt -tibial bolts in package instead of femoral bolts may delay procedure

Status: Terminated

Product Quantity: 21 units

Code Information:

Lot Number: 098780 UDI Number: (01) 00880304482739 (17) 290501 (10) 098780

Distribution Pattern:

Worldwide distribution - US Nationwide distribution in the state of FL and the countries of Korea, Japan, Netherlands.

Voluntary or Mandated:

Voluntary: Firm initiated