FDAJanuary 18, 2018device

Spinal Jaxx Interbody Fusion Device, Model: 100001-511, Size: 9 H x 10 W x 25 L Product Usage: The Spinal Jaxx interbody fusion device is indicated for spinal fusion for patients with degenerative disc disease (DDD) at one or two contiguous levels of the lumbosacral spine (L2-S1). DDD is defined ...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The implant size is incorrectly etched on the implant. The size listed on the box is correct.

What to do

FDA enforcement status: Terminated

Brands named

neuropro spinal jaxxneuroproneuropro spinal

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Spinal Jaxx Interbody Fusion Device, Model: 100001-511, Size: 9 H x 10 W x 25 L Product Usage: The Spinal Jaxx interbody fusion device is indicated for spinal fusion for patients with degenerative disc disease (DDD) at one or two contiguous levels of the lumbosacral spine (L2-S1). DDD is defined ... — Recall Details · AllClear