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Stryker Spine recalls AVS Aria Cage, Catalog Number 48753212 Product Usage: The Stryker Spine AVS¿ ARIA 1M PEEK Spacers are intervertebral
Recalled October 17, 2018 · FDA recall Z-0092-2019 · Stryker Spine
Hazard
The anterior and posterior markers on the cage were on the incorrect/opposite sides of the cage. · FDA Class II
Units
5
Sold at
US Nationwide in the states: CA, FL, GA, MI, MN, NJ, NM, and OR
Description
The anterior and posterior markers on the cage were on the incorrect/opposite sides of the cage.
Product
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.
Manufacturer(s)
Stryker Spine
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →