Z-1223-2021 Class II Ongoing
FDA device recall Z-1223-2021 was initiated by RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) on January 15, 2021 and is designated Class II. Reason for recall: Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision The recall status is ongoing.
Recall Details
- Product Type
- Devices
- Report Date
- March 17, 2021
- Initiation Date
- January 15, 2021
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
Product Description
CervAlign Anterior Cervical Plate System-Cervalign, 3Level, 51mm Material Number: 66-351 - 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).
Reason for Recall
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision
Distribution Pattern
US Nationwide distribution.
Code Information
Batch Number: 333021 333022 338840 341489 343445 346886 351527 351528 351528 351528 351528 351528 351528 358459 358459 358459 358459 358459 358459 362405 363444 364766 364766 369197 369197 370268 377838 377838 379930 379930 379930 379930 379931 379931 385407