Exact FDA event identifier

Event 68109

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

Open FDA event record

Event summary

Timeline bucket: January 08, 2014
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: The Anspach Effort, 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

ANSPACH Cutting bur, 3 mm Diamond Ball, Standard Length. REF L-3SD Use with LONG Attachments. Used for cutting and shaping bone, including the spine and cranium.

Z-1574-2014

Recall number: Z-1574-2014
Initiated: January 08, 2014
Classification: Class II
Status: Terminated
Recalling firm: The Anspach Effort, Inc.
Quantity: 30 cutting burs affected

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Anspach product code L-3SD contained product code S-3SD which is shorter in length than the labeled product.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling mix-ups

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Anspach product code L-3SD contained product code S-3SD which is shorter in length than the labeled product.

Code information

Lot/Set/Serial: G323081803.

Distribution pattern

Nationwide Distribution including FL, TX, NC, IL, CO, and PA.