Zimmer Spine, Inc.: Medical Device Recall in 2016 - (Recall #: Z-1019-2016)

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:

Virage OCT Spinal Fixation System. Intended to promote fusion of the Occipital-Cervical-Thoracic spine (Occiput-T3).

Product Classification:

Class II

Date Initiated: February 3, 2016

Date Posted: March 9, 2016

Recall Number: Z-1019-2016

Event ID: 73265

Reason for Recall:

Zimmer Biomet Spine is initiating a Medical Device Correction regarding the Virage OCT Spinal Fixation System by providing additional guidance in the Virage OCT Surgical Technique Manual.

Status: Terminated

Product Quantity: 15,753

Code Information:

Surgical Technique Manual L1637 Rev B (2014-06)

Distribution Pattern:

Distributed US (nationwide) and in the countries of Australia and Germany.

Voluntary or Mandated:

Voluntary: Firm initiated