Stryker Spine recalls AVS Aria Cage (Catalog 48753212) due to anterior and posterior markers being on the wrong sides, potentially causing surgical errors. Affected patients should contact Stryker for guidance.
The anterior and posterior markers on the cage were on the incorrect/opposite sides of the cage.
Stryker Spine is recalling AVS Aria Cage spacers with catalog number 48753212 because the anterior and posterior markers are on the incorrect sides. This could lead to surgical errors during spinal fusion procedures if the markers are misaligned.
The anterior and posterior markers on the cage are on the opposite sides of the cage than they should be. This could cause the surgeon to place the spacer incorrectly during spinal fusion surgery, leading to improper alignment of the spine.
Patients who have received the AVS Aria Cage spacers (catalog number 48753212) for spinal fusion surgery are affected. Surgeons and medical staff using these spacers during procedures are at higher risk.
Check for the catalog number 48753212 on the product label. The product is used in spinal fusion procedures for degenerative disc disease from L2 to S1.
Reach out to Stryker Spine directly for guidance on whether the cage is affected and next steps.
The anterior and posterior markers on the cage are on the incorrect sides, which could lead to surgical errors during spinal fusion procedures.
The catalog number for the recalled AVS Aria Cage is 48753212.
The recall does not specify a stop-use instruction; affected patients should contact Stryker Spine for guidance.
We’ve drafted a message you can send Stryker Spine to request your refund or repair — edit it as you like.
Subject: Recall Z-0092-2019 — Stryker Spine Stryker Spine Hello, I own a Stryker Spine that is covered by recall Z-0092-2019 from Stryker Spine. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
