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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 87251

41 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
January 15, 2021
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

41 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 1 Level, 10mm Material Number: 66-110 - 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-1204-2021
Recall number
Z-1204-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
65 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 328891, 328892

Distribution pattern

US Nationwide distribution.

device · product 2 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 1 Level, 12mm Material Number: 66-112 - 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-1205-2021
Recall number
Z-1205-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 328891 328893 328894 338794 340980 341495 344086 347925 347926 352672 358452 363412 363413 364047 367781 369328 370314 372189 372190 379399 379400 386003

Distribution pattern

US Nationwide distribution.

device · product 3 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 1 Level, 14mm Material Number: 66-114 - 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-1206-2021
Recall number
Z-1206-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 328895 328896 328897

Distribution pattern

US Nationwide distribution.

device · product 4 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 1 Level, 16mm Material Number: 66-116 - 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-1207-2021
Recall number
Z-1207-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 328898 328899

Distribution pattern

US Nationwide distribution.

device · product 5 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 1 Level, 18mm Material Number: 66-118 - 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-1208-2021
Recall number
Z-1208-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 329481 329482

Distribution pattern

US Nationwide distribution.

device · product 6 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 1 Level, 20mm Material Number: 66-120 - 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-1209-2021
Recall number
Z-1209-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 329483 338820 344091 348578 353381 363435 364051 367788 372225 372226 379406

Distribution pattern

US Nationwide distribution.

device · product 7 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 1 Level, 24m Material Number: 66-124 - 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-1210-2021
Recall number
Z-1210-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 329485 338822 341498 344093 348580 353383 363437 364053 369331 372220 379408

Distribution pattern

US Nationwide distribution.

device · product 8 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 2Level, 24mm Material Number: 66-224 - 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-1211-2021
Recall number
Z-1211-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 330510 330511 338826 344094 350507 355018 361793 361794 364054 372180 372181 377184 378427

Distribution pattern

US Nationwide distribution.

device · product 9 of 41

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).

Z-1212-2021
Recall number
Z-1212-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 330512 330513 338827 340984 344095 350509 350510 352675 361797 364055 364747 367798 370387 372182 377185 378428

Distribution pattern

US Nationwide distribution.

device · product 10 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 2Level, 28mm Material Number: 66-228 - 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-1213-2021
Recall number
Z-1213-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 330970 330971 338828 340985 344096 350511 350512 352676 355019 361799 364056 367799 369334 370389 372183 372184 378429 378430

Distribution pattern

US Nationwide distribution.

device · product 11 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 2Level, 32mm Material Number: 66-232 - 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-1214-2021
Recall number
Z-1214-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 330973 330975 330976 338830 338831 344099 344100 350516 350517 356798 358456 361803 361804 364749 369336 370393 377188 379018 379542 379543 379544 380874

Distribution pattern

US Nationwide distribution.

device · product 12 of 41

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
Recall number
Z-1215-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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.

device · product 13 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 2Level, 36mm Material Number: 66-236 - 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-1216-2021
Recall number
Z-1216-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 332500 338833 344102 350520 353384 361807 364751 364752 369338 377190 379080 380872

Distribution pattern

US Nationwide distribution.

device · product 14 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 2Level, 38mm Material Number: 66-238 - 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-1217-2021
Recall number
Z-1217-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 332504 338834 344103 350521 353385 361808 364753 367807 370398 379081

Distribution pattern

US Nationwide distribution.

device · product 15 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 2Level, 40mm Material Number: 66-240 - 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-1218-2021
Recall number
Z-1218-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 332505 338835 344104 350522 354403 361810 367193 370399 379082

Distribution pattern

US Nationwide distribution.

device · product 16 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 2Level, 42mm Material Number: 66-242 - 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-1219-2021
Recall number
Z-1219-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 332506 338836 342573 344105 350523 361814 364756 366089 369339 379083

Distribution pattern

US Nationwide distribution.

device · product 17 of 41

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).

Z-1220-2021
Recall number
Z-1220-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 333014 333016 338837 341887 343444 346882 351523 355020 361818 364757 367810 369360 370401 372233 379926

Distribution pattern

US Nationwide distribution.

device · product 18 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 3 Level, 45mm Material Number: 66-345 - 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-1221-2021
Recall number
Z-1221-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 333017 333018 338838 346883 346884 351525 354404 358458 359841 364531 369361 370402 377835 377836 379927

Distribution pattern

US Nationwide distribution.

device · product 19 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 3 Level, 48mm Material Number: 66-348 - 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-1222-2021
Recall number
Z-1222-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 333019 333020 338839 341491 346885 351526 354405 359842 359843 363443 364532 369362 370404 377837 379929 385416

Distribution pattern

US Nationwide distribution.

device · product 20 of 41

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).

Z-1223-2021
Recall number
Z-1223-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

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

Distribution pattern

US Nationwide distribution.

device · product 21 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 3Level, 54mm Material Number: 66-354 - 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-1224-2021
Recall number
Z-1224-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 333150 338842 341492 347125 351529 351530 358480 359845 364533 367814 369363 370406 377839 380043 380044 381527 381528 382443 382444 382445

Distribution pattern

US Nationwide distribution.

device · product 22 of 41

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).

Z-1225-2021
Recall number
Z-1225-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 333152 333152 338845 341493 347126 351531 355537 359848 364534 364971 369364 370407 378060 380152

Distribution pattern

US Nationwide distribution.

device · product 23 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 3Level, 60mm Material Number: 66-360 - 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-1226-2021
Recall number
Z-1226-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 333153 338846 341494 347127 351532 359849 364535 364767 369365 370408 378061 380153

Distribution pattern

US Nationwide distribution.

device · product 24 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 3Level, 63mm Material Number: 66-363 - 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-1227-2021
Recall number
Z-1227-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 333154 338847 341490 347128 351533 359850 364536 367817 370409 378062 380154

Distribution pattern

US Nationwide distribution.

device · product 25 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 4Level, 60mm Material Number: 66-460 - 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-1228-2021
Recall number
Z-1228-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 342452 348027 351950 357125 364537 380155 380156 385417

Distribution pattern

US Nationwide distribution.

device · product 26 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 4Level, 64mm Material Number: 66-464 - 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-1229-2021
Recall number
Z-1229-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 342453 348028 351951 357126 364538 370411 380157

Distribution pattern

US Nationwide distribution.

device · product 27 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 4Level, 68mm Material Number: 66-468 - 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-1230-2021
Recall number
Z-1230-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 342454 348029 351952 357127 364539 370412 380678

Distribution pattern

US Nationwide distribution.

device · product 28 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 4Level, 72mm Material Number: 66-472 - 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-1231-2021
Recall number
Z-1231-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 342455 348030 351953 356880 359851 380679 380680 385418

Distribution pattern

US Nationwide distribution.

device · product 29 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 4Level, 76mm Material Number: 66-476 - 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-1232-2021
Recall number
Z-1232-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 342456 348031 351954 357128 364540 370414 381213 381525 383204

Distribution pattern

US Nationwide distribution.

device · product 30 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 4Level, 80mm Material Number: 66-480 - 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-1233-2021
Recall number
Z-1233-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 342457 348032 351955 357129 364769 381292

Distribution pattern

US Nationwide distribution.

device · product 31 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 4Level, 84mm Material Number: 66-484 - 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-1234-2021
Recall number
Z-1234-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 342458 348033 351956 357130 364770 370416 381526

Distribution pattern

US Nationwide distribution.

device · product 32 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 4Level, 88mm Material Number: 66-488 - 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-1235-2021
Recall number
Z-1235-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 342459 348034 351957 357131 364771 381524 385440

Distribution pattern

US Nationwide distribution.

device · product 33 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 5 Level, 100mm Material Number: 66-5100 - 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-1236-2021
Recall number
Z-1236-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 345227 352382 357123 364541 372302 382119

Distribution pattern

US Nationwide distribution.

device · product 34 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 5 Level, 105mm Material Number: 66-5105 - 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-1237-2021
Recall number
Z-1237-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 345228 352383 357124 364542 370440 382120

Distribution pattern

US Nationwide distribution.

device · product 35 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 5 Level, 75mm Material Number: 66-575 - 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-1238-2021
Recall number
Z-1238-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 345222 352337 357118 364543 372238 382115 386005

Distribution pattern

US Nationwide distribution.

device · product 36 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 5 Level, 80mm Material Number: 66-580 - 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-1239-2021
Recall number
Z-1239-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 345223 352338 357119 372239 382116

Distribution pattern

US Nationwide distribution.

device · product 37 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 5 Level, 85mm Material Number: 66-585 - 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-1240-2021
Recall number
Z-1240-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 345224 352339 357120 364544 370418 382117

Distribution pattern

US Nationwide distribution.

device · product 38 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 5 Level, 90mm Material Number: 66-590 - 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-1241-2021
Recall number
Z-1241-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 345225 352380 357121 359852 370419 382118

Distribution pattern

US Nationwide distribution.

device · product 39 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 5 Level, 95mm Material Number: 66-595 - 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-1242-2021
Recall number
Z-1242-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 345226 352381 357122 369366 372235 381293

Distribution pattern

US Nationwide distribution.

device · product 40 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 1 Level, 22mm Material Number: 66-122 - 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-1243-2021
Recall number
Z-1243-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 329484 338821 341497 344092 348579 353382 363436 367789 372223 372224 379407

Distribution pattern

US Nationwide distribution.

device · product 41 of 41

CervAlign Anterior Cervical Plate System-Cervalign, 2Level, 30mm Material Number: 66-230 - 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-1244-2021
Recall number
Z-1244-2021
Initiated
January 15, 2021
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Batch Number: 330972 330973 338829 344097 344098 350514 350515 352677 358455 361801 361802 364748 367803 369335 370391 370392 377187 379016 379539 379540 379541

Distribution pattern

US Nationwide distribution.