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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 64245

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

Open FDA event record

Event summary

Timeline bucket
February 04, 2013
Product types
Food
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Aptalis Pharma Us Inc

Dossier provenance

Source snapshots represented here

  • openFDA Food 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.

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.

food · product 1 of 1

SourceCF(R) Pediatric Drops, Multivitamins with A, B, D, E and K Plus Zinc, 2 FL OZ. (60ML), NDC 66212-300-60, UPC 668212300600

F-1008-2013
Recall number
F-1008-2013
Initiated
February 04, 2013
Classification
Class II
Status
Terminated
Recalling firm
Aptalis Pharma Us Inc
Quantity
14439 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The data suggests that the formulation does not support the shelf life of the product as labeled.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

The data suggests that the formulation does not support the shelf life of the product as labeled.

Code information

1BA67, exp Mar 13; 1DC02, exp Jun 13; 2BA86, exp Apr 14; 2FA92, exp Aug13.

Distribution pattern

Nationwide, Italy, Canada, and Brazil