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Synthes, Inc. recalls Hemostatic Bone Putty, for use as a water-soluble implant material and for use in the control of bleeding from bone sur
Recalled February 18, 2015 · FDA recall Z-1094-2015 · Synthes
Hazard
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. · FDA Class II
Units
38
Sold at
Distributed in the state of WI
Description
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.
Product
Hemostatic Bone Putty, for use as a water-soluble implant material and for use in the control of bleeding from bone surfaces.
Manufacturer(s)
Synthes, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →