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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 67176

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

Open FDA event record

Event summary

Timeline bucket
March 31, 2011
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

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

AnspacSingle use Sterile bone cutting burs.h REF: S-1504TD Twist Drill for 1.5mm x 4mm screw. Rx only Single use Sterile bone cutting burs.

Z-0829-2014
Recall number
Z-0829-2014
Initiated
March 31, 2011
Classification
Class II
Status
Terminated
Recalling firm
The Anspach Effort, Inc.
Quantity
599 cutting burs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Cutter was longer than was stated on the label

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

Cutter was longer than was stated on the label

Code information

Lot #'s: D293037349, D323038110 and D363039140

Distribution pattern

Worldwide Distribution - USA including CA, CO, IN, KY, MD and TX and Internationally to Japan, Taiwan, United Kingdom, Sweden, and Germany.

device · product 2 of 2

Anspach REF: TURQ-434-4 Twist Drill for 1.5mm x 4mm screw. Rx only Single use Sterile bone cutting burs.

Z-0830-2014
Recall number
Z-0830-2014
Initiated
March 31, 2011
Classification
Class II
Status
Terminated
Recalling firm
The Anspach Effort, Inc.
Quantity
29 cutting burs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Cutter was longer than was stated on the label

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

Cutter was longer than was stated on the label

Code information

Lot #'s: D323038131 and D343038845

Distribution pattern

Worldwide Distribution - USA including CA, CO, IN, KY, MD and TX and Internationally to Japan, Taiwan, United Kingdom, Sweden, and Germany.