Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hemostatic Bone Putty Recalled by Synthes, Inc. Due to Revision A of the Hemostatic Bone Putty Brochure...
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 Synthes, Inc. directly.
Affected Products
Hemostatic Bone Putty, for use as a water-soluble implant material and for use in the control of bleeding from bone surfaces.
Quantity: 38
Why Was This Recalled?
Revision A of the Hemostatic Bone Putty Brochure (J10847A) was sent to sales consultants instead of Revision B (J10847B), which corrected an error in the indication statement.
Where Was This Sold?
This product was distributed to 1 state: WI
About Synthes, Inc.
Synthes, Inc. has 43 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report