Stryker Howmedica Osteonics Corp.: Medical Device Recall in 2016 - (Recall #: Z-0855-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Stryker Vitallium Wire (6 Pack) Non Sterile. For use in bone procedures.

Product Classification:

Class II

Date Initiated: December 23, 2015

Date Posted: March 2, 2016

Recall Number: Z-0855-2016

Event ID: 73042

Reason for Recall:

The wire packages are correctly marked with a "NON-STERILE" label, however, the enclosed Instructions For Use (IFU) states the device are sterilized via gamma irradiation and should not be resterilized. Since the IFU states the devices are sterile, no instructions for moist heat sterilization are provided.

Status: Terminated

Product Quantity: 3,741 units

Code Information:

All lots of the following Catalog Numbers: 2704-1-024; 2704-3-018; 6703-1-018; 6703-2-120; 6704-1-018; 6704-2-120 and 6704-3-120.

Distribution Pattern:

Nationwide Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated