Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0092-2019 — 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¿ AR

U.S. FDA — Device Enforcement · United States · 2018-08-13 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0092-2019
Date of alert: 2018-08-13
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Stryker Spine
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 48753212

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

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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