FDAClass IIMarch 17, 2021

CervAlign Anterior Cervical Plate System-Cervalign recall

CervAlign Anterior Cervical Plate System-Cervalign, 3 Level, 48mm Material Number: 66-348 - Product Usage: intended for anterior cervical fixation…

Why was CervAlign Anterior Cervical Plate System-Cervalign recalled?

Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Batch Number: 333019 333020 338839 341491 346885 351526 354405 359842 359843 363443 364532 369362 370404 377837 379929 385416

Product
CervAlign Anterior Cervical Plate System-Cervalign, 3 Level, 48mm Material Number: 66-348 - Product Usage: intended for anterior cervical fixation…
Recalling firm
RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
Distribution
US Nationwide distribution.
Recall date
March 17, 2021
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls