Exact FDA event identifier

Event 71940

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

Open FDA event record

Event summary

Timeline bucket: August 05, 2015
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Biomet Spine, LLC

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

Biomet Parsippany, NJ. 4 0 MM X 14 MM Variable Screw C-Tek Maxan Anterior Cervical Plate System. Lot 375440.

Z-2744-2015

Recall number: Z-2744-2015
Initiated: August 05, 2015
Classification: Class II
Status: Terminated
Recalling firm: Biomet Spine, LLC
Quantity: 7 parts

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

mislabeled

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

Some of P/N 14-521614B Lot 375440 was mislabeled as P/N 14-521614 Lot 375440.

Code information

Model Number 14-521614B, lot number 375440.

Distribution pattern

Nationwide Distribution including Distributed nationwide to OH, LA, TX, and GA.