Zimmer Biomet, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1495-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Orthosize Templating Version 1.2.6 Echo Bi-Metric Hip Stem Digital Templates. For preoperative planning of orthopedic surgery.

Product Classification:

Class II

Date Initiated: February 14, 2017

Date Posted: March 29, 2017

Recall Number: Z-1495-2017

Event ID: 76442

Reason for Recall:

Digital templates were created with the incorrect files.

Status: Terminated

Product Quantity: 3232

Code Information:

Orthosize Templating Version 1.2.6

Distribution Pattern:

Worldwide distribution. US Nationwide including Puerto Rico, Canada, Argentina, Australia, Austria, Belgium, Chile, China, Denmark, Finland, France, Germany, Greece, India, Italy, Japan, Korea, Lithuania, Malaysia, Mexico, Netherlands, Nicaragua, Norway, Pakistan, Poland, Portugal, Romania, Singapore, South Africa, Spain, Sweden, Switzerland, Turkey, United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated