medical Class II Updated 2021-03-17

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

Recalled Product

CervAlign Anterior Cervical Plate System-Cervalign, 3 Level, 42mm Material Number: 66-342 - 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: 333014 333016 338837 341887 343444 346882 351523 355020 361818 364757 367810 369360 370401 372233 379926
View official government recall

Looking for safe alternatives?

Browse certified-safe products in this category on Amazon →