Exact FDA event identifier

Event 82587

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

Event summary

Timeline bucket: April 08, 2019
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: DePuy 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

2 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 2

Concorde Lift, Expandable Interbody Device, spinal fusion implant Convex 9x21 (197809021C), 9x26 (197809026C), 11x21 (197811021C), 11x26 (197811026C), 9x21 (US197809021C), 9x26 (US197809026C)

Z-1225-2019

Recall number: Z-1225-2019
Initiated: April 08, 2019
Classification: Class II
Status: Terminated
Recalling firm: DePuy Spine, Inc.
Quantity: 3166 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

A complaint trend was observed for post-operative loss of height and migration for Concorde Lift G3+ implants.

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

A complaint trend was observed for post-operative loss of height and migration for Concorde Lift G3+ implants.

Code information

All lots

Distribution pattern

US Nationwide distribution. Foreign distribution to Austria, Switzerland, and United Kingdom.

device · product 2 of 2

Concorde Lift, Lordotic Expandable Interbody Device, spinal fusion implant 9x23 (197809023L), 9x27 (197809027L), 11 x 23 (197811023L), 11x27 (197811027L), 9x23 (US197809023L), 9x27 (US197809027L)

Z-1226-2019

Recall number: Z-1226-2019
Initiated: April 08, 2019
Classification: Class II
Status: Terminated
Recalling firm: DePuy Spine, Inc.
Quantity: 3166 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

A complaint trend was observed for post-operative loss of height and migration for Concorde Lift G3+ implants.

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

A complaint trend was observed for post-operative loss of height and migration for Concorde Lift G3+ implants.

Code information

All lots

Distribution pattern

US Nationwide distribution. Foreign distribution to Austria, Switzerland, and United Kingdom.