Stryker Spine: Medical Device Recall in 2018 - (Recall #: Z-0092-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

AVS Aria Cage, Catalog Number 48753212 Product Usage: The Stryker Spine AVS¿ ARIA 1M PEEK Spacers are intervertebral body fusion devices indicated for use with autogenous bone graft in patients with degenerative disc disease (DDD) at one level or two contiguous levels from L2 to S1 . The AVS¿ ARIA TM PEEK Spacers are intended to be used with supplemental fixation systems that have been cleared for use in the lumbosacral spine.

Product Classification:

Class II

Date Initiated: August 13, 2018

Date Posted: October 17, 2018

Recall Number: Z-0092-2019

Event ID: 80971

Reason for Recall:

The anterior and posterior markers on the cage were on the incorrect/opposite sides of the cage.

Status: Terminated

Product Quantity: 5

Code Information:

Lot Number 7HX

Distribution Pattern:

US Nationwide in the states: CA, FL, GA, MI, MN, NJ, NM, and OR

Voluntary or Mandated:

Voluntary: Firm initiated