Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vanguard 360 Femoral Boss Reamer Recalled by Biomet, Inc. Due to The Vanguard 360 Femoral Boss Reamers were manufactured...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Biomet, Inc. directly.
Affected Products
Vanguard 360 Femoral Boss Reamer, Label: REF 32-488474 VANGUARD 360 1NSTRUMENT FEMORAL BOSS REAMER NON-STERILE, BIOMET ORTHOPEDICS 56 EAST BELL DRIVE P.O. BOX 587 WARSAW, IN 46581 USA
Quantity: 461
Why Was This Recalled?
The Vanguard 360 Femoral Boss Reamers were manufactured oversized to the print. The instrument may not fit into the mating component.
Where Was This Sold?
This product was distributed to 16 states: AL, AR, CO, FL, GA, IL, IA, KS, MD, MA, NV, NH, OK, SC, UT, WA
About Biomet, Inc.
Biomet, Inc. has 250 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report