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Recall Observatory FDA recall evidence

Device product

CervAlign Anterior Cervical Plate System-Cervalign, 2Level, 34mm Material Number: 66-234 - 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).

Z-1215-2021

January 15, 2021

Class II

Product summary

Firm
RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
Event
Event 87251
Status
Ongoing
Classification
Class II
Quantity
Unavailable
Official record key
device-enforcement:Z-1215-2021

Official wording

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

Code information: Batch Number: 330976 330977 330978 338832 343961 344101 350518 350519 356799 358457 361805 361806 364750 367806 369337 370395 377189 379019 380051 380052 380053 380054 380055 380056 380687 380688 380689

Distribution pattern: US Nationwide distribution.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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