Neuropro Spinal Jaxx Spinal Jaxx Interbody Fusion Device, Model: 100001-511, Size: 9 H x 10 recall — FDA Z-1350-2018
The implant size is incorrectly etched on the implant. The size listed on the box is correct.
Overview of recall records associated with Neuropro Spinal Jaxx, including dates, categories and classifications where available.
Classification mix: Class II: 1.
The implant size is incorrectly etched on the implant. The size listed on the box is correct.
This page summarizes recall records in which the official source identifies Neuropro Spinal Jaxx as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.