Synthes, Inc.: Medical Device Recall in 2015 - (Recall #: Z-1094-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Hemostatic Bone Putty, for use as a water-soluble implant material and for use in the control of bleeding from bone surfaces.

Product Classification:

Class II

Date Initiated: January 6, 2012

Date Posted: February 18, 2015

Recall Number: Z-1094-2015

Event ID: 70055

Reason for Recall:

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.

Status: Terminated

Product Quantity: 38

Code Information:

Part 10847A

Distribution Pattern:

Distributed in the state of WI

Voluntary or Mandated:

Voluntary: Firm initiated