Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AlloFuse DBM Putty 5cc Recalled by AlloSource, Inc. Due to The donor was hemodiluted.
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 AlloSource, Inc. directly.
Affected Products
AlloFuse DBM Putty 5cc, Catalog No. 90038005 AlloFuse is indicated for orthopedic applications as filler for gaps or voids that are not intrinsic to the stability of the bony structure. AlloFuse is indicated to be packed gently into bony gaps in the skeletal system as a bone graft extender.
Quantity: 29
Why Was This Recalled?
The donor was hemodiluted.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About AlloSource, Inc.
AlloSource, Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report