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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 69419

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

Open FDA event record

Event summary

Timeline bucket
September 10, 2014
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Intertrade Imports 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

Labeled in part: I Color Complete / Color Lens, blister packing, 14.5mm. (Additional colors include: 1) Illusion style, Chestnut Brown, Violet and others and 2) 2 Tone style: like Misty Blue among others)Eye contact lens Product Usage - Eye contact lens

Z-0950-2015
Recall number
Z-0950-2015
Initiated
September 10, 2014
Classification
Class II
Status
Terminated
Recalling firm
Intertrade Imports Inc.
Quantity
750 units

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
presence of Bacillus Cereus

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Material/Component Contamination

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

A surveillance sample collected by FDA confirmed the presence of Bacillus Cereus and Bacillus Lentus in the contact lenses. I Color Color Complete brand color contact lenses are unapproved medical devices.

Code information

ALL LOTS / CODES

Distribution pattern

Worlldwide Distribution - USA including Texas, California, Florida, and St. Lucia, Barbados and St. Marten.

device · product 2 of 2

Labeled in part: I Color Complete / Crazy Lens, blister packing, 14.5mm, (Additional colors include: #003 White out, #005 Yellow out, #020 Red out, #014 Black out, #070 Manson, #136 Lava, #009 Yellow cat, #073 Red cat, #050 White cat, #032 Soccer ball, #077 Spiral, #071 Target, #057 Wild fire, #056 Spider web, #174 Black moon, #179 Green moon, #180 Zombie, #181 Green hole, and #184 Black hole among others styles) Product Usage - Eye contact lens

Z-0951-2015
Recall number
Z-0951-2015
Initiated
September 10, 2014
Classification
Class II
Status
Terminated
Recalling firm
Intertrade Imports Inc.
Quantity
2850 each

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
presence of Bacillus Cereus

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Material/Component Contamination

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

A surveillance sample collected by FDA confirmed the presence of Bacillus Cereus and Bacillus Lentus in the contact lenses, product is not sterile. I Color Color Complete brand color contact lenses are unapproved medical devices.

Code information

ALL LOTS / CODES

Distribution pattern

Worlldwide Distribution - USA including Texas, California, Florida, and St. Lucia, Barbados and St. Marten.