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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 62624

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

Open FDA event record

Event summary

Timeline bucket
July 19, 2012
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Laserworld Usa 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

Laserworld RGB & Piko Nano RGB Models All models are laser light show projectors, and will be used as such.

Z-1538-2013
Recall number
Z-1538-2013
Initiated
July 19, 2012
Classification
Class II
Status
Terminated
Recalling firm
Laserworld Usa Inc
Quantity
Total distribution of more than 500 units between July1, 2008, and June 30, 2012

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
A potential lack of certification, and/or missing laser certification, laser safety warning and administrative labels, and potentially incomplete Performance Feature set and incomplete User Information were discovered.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Radiation Control for Health and Safety Act

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

A potential lack of certification, and/or missing laser certification, laser safety warning and administrative labels, and potentially incomplete Performance Feature set and incomplete User Information were discovered.

Code information

All projectors distributed between 2008 and 2012, including, but not limited to, the Proline Series AG, Revolution Series AG, Club Series AG, Clus Series, Pure Light Series, and Revolution Series AG

Distribution pattern

US Distribution including the states of CA, CO, FL, KS and PA.