Exact FDA event identifier

Event 66536

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

Open FDA event record

Event summary

Timeline bucket: September 19, 2013
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Aesculap, 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

Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7

Z-0492-2014

Recall number: Z-0492-2014
Initiated: September 19, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aesculap, Inc.
Quantity: 24

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

The Columbus Revision CoCr 15 mm distal and posterior implant spacers, sizes F5-F7, were not compatible.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Component change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Columbus Revision CoCr 15 mm distal and posterior implant spacers, sizes F5-F7, were not compatible.

Code information

lots: 51468773, 51447588, 51468302, 51503760, 51571394, 51585136, 51447597

Distribution pattern

Distributed in FL and MD.