medical Class II Updated 2021-03-17

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) recalls CervAlign Anterior Cervical Plate System-Cervalign, 3Level,

Recalled Product

CervAlign Anterior Cervical Plate System-Cervalign, 3Level, 57mm Material Number: 66-357 - 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: 333152 333152 338845 341493 347126 351531 355537 359848 364534 364971 369364 370407 378060 380152
View official government recall

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