Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stryker Aria Implant Inserter Recalled by Stryker Spine Due to Stryker has initiated the recall of its Aria...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Stryker Spine directly.
Affected Products
Stryker Aria Implant Inserter, REF 48758500, This instrument is part of the Aria product brand. It is used for Implant insertion into the disc space. The Aria Inserter PEEK Spacer System offers implants that are interbody fusion devices intended for use as an aid in spinal fixation. These hollow implants are offered in a variety of lengths, heights, and lordotic angles designed to adapt to different patient anatomies. They have serrations on the superior and inferior surfaces designed for multidirectional fixation, ergonomically shaped anterior edges, and flat posterior edges. This device does not sustain or support life.
Quantity: 64 units
Why Was This Recalled?
Stryker has initiated the recall of its Aria Standard and Specialty Implant Inserters due to complaints of product fracturing.
Where Was This Sold?
This product was distributed to 24 states: AL, AZ, CA, CO, FL, GA, IN, IA, KS, MD, MA, MI, MN, MO, MT, NY, OH, OK, OR, PA, TN, TX, UT, WI
About Stryker Spine
Stryker Spine has 29 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report