Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Globus Medical MicroFuse Putty Recalled by Globus Medical, Inc. Due to The sterility of this product to a Sterility...
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 Globus Medical, Inc. directly.
Affected Products
Globus Medical MicroFuse Putty, 2.5cc and 10cc. Product Usage: MicroFuse Bone Void Filler is indicated only for bony voids or gaps that are not intrinsic to the stability of the bony structure. MicroFuse Bone Void Filleris a bone graft extender to be used with autogenous bone marrow aspirate or autograft
Quantity: 193
Why Was This Recalled?
The sterility of this product to a Sterility Assurance Level (SAL) of 10(-6) cannot be assured.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Globus Medical, Inc.
Globus Medical, Inc. has 29 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report