FDAMarch 5, 2021device

Prodisc C - prosthesis, intervertebral disc - Product Usage: indicated in skeletally mature patients for reconstruction of the disc from C3-C7 following single-level discectomy for intractable symptomatic cervical disc disease (SCDD), Part number: 09.820.055S

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

The hazard

Centinel Spine learned through five customer complaints that the product was missing the "UP" etching on the superior plate of the prodisc C device. Per the Surgical Technique, the "UP" is one of the methods used to indicate the direction in which the surgeon should place the prodisc C into intradiscal space. There are also "UP" indications in the packaging and on instrumentation as additional guides to help the surgeon properly implant the device that were present for the affected product.

What to do

FDA enforcement status: Terminated

Brands named

centinel spinecentinel

UPCs

00843193112842

Recall history

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

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