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Biomet, Inc. recalls Vanguard 360 Revision System Posterior Augment With Bolt - Product Usage: intended for use in knee arthroplasty Item
Recalled December 30, 2020 · FDA recall Z-0723-2021 · Biomet
Hazard
Incorrect bolt -tibial bolts in package instead of femoral bolts may delay procedure · FDA Class II
Units
21 units
Sold at
Worldwide distribution - US Nationwide distribution in the state of FL and the countries of Korea, Japan, Netherlands.
Description
Incorrect bolt -tibial bolts in package instead of femoral bolts may delay procedure
Product
Vanguard 360 Revision System Posterior Augment With Bolt - Product Usage: intended for use in knee arthroplasty Item Number: 185422
Manufacturer(s)
Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →