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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 63633

1 recalled-product record grouped only because every row carries this exact official event ID.

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Event summary

Timeline bucket
September 20, 2012
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Captiva Spine, 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

1 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 1

CapLOX II Final Torque Driver, Indicator is a Pedicle screw spinal system. The CapLOX II Spinal System is a posterior, non-cervical pedicle fixation system intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities of the thoracic, lumbar, and sacral spine including degenerative spondylolisthesis with objective evidence of neurologic impairment, fracture, dislocation, scoliosis, kyphosis, spinal tumor, pseudoarthrosis and failed previous fusion.

Z-0413-2013
Recall number
Z-0413-2013
Initiated
September 20, 2012
Classification
Class II
Status
Terminated
Recalling firm
Captiva Spine, Inc
Quantity
10

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Captiva Spine recalled their CapLOX II Final Torque Driver, Indicator due to the device prematurely breaking

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Captiva Spine recalled their CapLOX II Final Torque Driver, Indicator due to the device prematurely breaking

Code information

Model # 2201-5004, Lot # 06110093 Devices are also seialized as 101-110.

Distribution pattern

Nationwide Distribution (Distributed to one customer located in MN)