FDAJanuary 7, 2019device

A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Link Z Ti Unitary Open Interbody 32x24x12 7 A Link Z Ti Unitary Open Interbody 32x24x12 12 A Link Z Ti Unitary Open Interbody 32x24x16 7 A Link Z Ti Unitary Open Interbody 32x24x16 12 Product Usage: is a spinal device that is impla...

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

The hazard

Due to a manufacturing process issue, it allowed vertebral body bone screws to not seat properly within the spinal device/cage.

What to do

FDA enforcement status: Ongoing

Brands named

acuity surgical devicesacuityacuity surgical

Recall history

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

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