Exact FDA event identifier

Event 65483

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

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Event summary

Timeline bucket: June 19, 2013
Product types: Device
Classifications: Class III
Statuses: Terminated
Recalling firm wording: Beekley Corporation

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

Beekley Spots Light Image O-Spots for Mammography Catalog Number: 252 Product Usage: To identify raised moles in Mammography

Z-1787-2014

Recall number: Z-1787-2014
Initiated: June 19, 2013
Classification: Class III
Status: Terminated
Recalling firm: Beekley Corporation
Quantity: 81 boxes

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

Error in labeling

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Light Image O-Spots Dispenser mislabeled as Soft n' Stretchy Light Image S-Spots

Code information

Lot Number: 252.04261301

Distribution pattern

Worldwide Distribution - USA in the states of CA, FL, MA, NC, NY, and PA.