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Recall Observatory FDA recall evidence

Device product

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.

Z-2626-2014

July 07, 2014

Class II

Product summary

Firm
Stryker Spine
Event
Event 68908
Status
Terminated
Classification
Class II
Quantity
64 units
Official record key
device-enforcement:Z-2626-2014

Official wording

Reason: Stryker has initiated the recall of its Aria Standard and Specialty Implant Inserters due to complaints of product fracturing.

Code information: Catalog #48758500, Lot #'s 107400, 10G906 and 110214;

Distribution pattern: Worldwide Distribution - USA including OR, AZ, TN, MA, MD, GA, FL, NY, IA, IN, TX, MI, PA, UT, CA, MN, MO, OH, KS, OK, MT, FL, AL, CO, TN, and WI and Internationally to Australia.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Stryker has initiated the recall of its Aria Standard and Specialty Implant Inserters due to complaints of product fracturing.