Exact FDA event identifier

Event 79072

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

Event summary

Timeline bucket: July 26, 2017
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: DePuy Orthopaedics, 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 Driver Shaft AO. Used with supplemental internal spinal fixation systems that have been cleared for use in the lumbar spine.

Z-0848-2018

Recall number: Z-0848-2018
Initiated: July 26, 2017
Classification: Class II
Status: Terminated
Recalling firm: DePuy Orthopaedics, Inc.
Quantity: 130 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Potential for Intra-operative breakage of driver tips

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

Potential for Intra-operative breakage of driver tips

Code information

Product code: 287804101G Lot number: 052316-A R, 121416-A R

Distribution pattern

Nationwide Distribution

device · product 2 of 2

Concorde Lift Torque Limiting Handle. Must be used with supplemental internal spinal fixation systems that have been cleared for use in the lumbar spine.

Z-0849-2018

Recall number: Z-0849-2018
Initiated: July 26, 2017
Classification: Class II
Status: Terminated
Recalling firm: DePuy Orthopaedics, Inc.
Quantity: 130 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Potential for Intra-operative breakage of driver tips

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

Potential for Intra-operative breakage of driver tips

Code information

Product code: 287804102 Lot number: 122315-B R, 122315-A R, 041117A

Distribution pattern

Nationwide Distribution