Zimmer Biomet, Inc.: Medical Device Recall in 2020 - (Recall #: Z-0570-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System, Thoracolumbosacral pedicle screw system

Product Classification:

Class II

Date Initiated: November 17, 2020

Date Posted: December 23, 2020

Recall Number: Z-0570-2021

Event ID: 86762

Reason for Recall:

Zimmer Biomet is conducting a medical device correction to update the Instructions for Use (IFU) and the Surgical Techniques for the Polaris Spinal System Translation Screw and Cypher MIS Screw System. Users should be aware that changes were made to the contraindications section indicating that the Translation Screws should not be used with a direct current stimulation, as a high probability of construct failure exists when using Translation Screws containing CoCr with direct current simulation system.

Status: Terminated

Product Quantity: 57,715 units

Code Information:

There have been 756 item numbers cleared in the US that are included in the recall scope, as listed on the first tab of the attached ZFA 2020-00333 Affected Product List. To date, there have only been products manufactured for a portion of the affected item numbers. In addition, there are three kit part numbers affected as well. The lot specific information is included on the second tab of the attached ZFA 2020- 0333 Affected Product List.

Distribution Pattern:

Domestic distribution nationwide. As direct stimulation devices are only available in the US, this contraindication does not apply to international customers.

Voluntary or Mandated:

Voluntary: Firm initiated