Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PerFuse Decompression Instrument PN: 800-0541 Recalled by Biomet, Inc. Due to The Trocar and Plunger Assemblies are missing from...
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
PerFuse Decompression Instrument PN: 800-0541, Lot:100650. Designed to access the femoral head for decompression.
Quantity: 22
Why Was This Recalled?
The Trocar and Plunger Assemblies are missing from the instrument, which could result in a delay in surgery greater than 30 minutes.
Where Was This Sold?
This product was distributed to 4 states: CA, GA, MN, OH
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