medical Class II Updated 2021-03-17

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) recalls CervAlign Anterior Cervical Plate System-Cervalign, 2Level,

Recalled Product

CervAlign Anterior Cervical Plate System-Cervalign, 2Level, 26mm Material Number: 66-226 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as neck pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies, spondylolisthesis, trauma (i.e. fracture or dislocation), spinal stenosis, deformities or curvatures (i.e. scoliosis, kyphosis, and/or lordosis), tumor, pseudathrosis, and failed previous fusion).


Hazard / Issue

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

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Batch Number: 330512 330513 338827 340984 344095 350509 350510 352675 361797 364055 364747 367798 370387 372182 377185 378428
View official government recall

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