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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 69021

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

Open FDA event record

Event summary

Timeline bucket
August 06, 2014
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Ellex iScience, 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

iTRACK250A Canaloplasty Microcatheter Kit; Catalogue number: iT-250A; Rx only, sterile. Indicated for fluid infusion and aspiration during surgery.

Z-2590-2014
Recall number
Z-2590-2014
Initiated
August 06, 2014
Classification
Class II
Status
Terminated
Recalling firm
Ellex iScience, Inc.
Quantity
148 devices

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
One lot may not have been properly sealed, resulting in a non-sterile device.

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

One lot may not have been properly sealed, resulting in a non-sterile device.

Code information

Lot number 1404-03; Expiration: March 31, 2016

Distribution pattern

Worldwide Distribution -- US (nationwide) and countries of: Hong Kong and Switzerland.