PlainRecalls
ModerateClass IITerminated

FDA Food recall · Reported March 6, 2013

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

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

Recall #
F-1008-2013
Affected scope
14439 units
Initiated
February 4, 2013
Verify with FDA Food →
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Aptalis Pharma Us Inc recalled SourceCF(R) Pediatric Drops, Multivitamins with A, B, D, E and K Plus Zinc, 2 FL OZ. (60M… - a moderate-severity action.

SourceCF(R) Pediatric Drops, Multivitamins with A, B, D, E and K Plus Zinc, 2 FL OZ. (60M… was recalled by Aptalis Pharma Us Inc in March 6, 2013. Reason: The data suggests that the formulation does not support the shelf life of the product as labeled.. Check the official notice for the remedy. Verify recall #F-1008-2013 with the FDA Food before acting.

The recall

Aptalis Pharma Us Inc issued this moderate-severity FDA Food recall-The data suggests that the formulation does not support the shelf life of the product as labeled..

Moderate
severity level
14K units
affected scope
Class II
classification
March 6, 2013
reported

Sourced from official FDA Food enforcement records. Verify recall #F-1008-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Household Products recalls over time

Where this recall sits in its category - 3,089 household products recalls on record

50100150200250 20052008201120142017202020232026 148
Severity1906864652High severity (most serious)Moderate severityLow severity
Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

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

Reason for recall

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

Recall Profile

Structured summary of the FDA Food recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Terminated
Recall number F-1008-2013
Date reported March 6, 2013
Date initiated February 4, 2013
Recalling firm Aptalis Pharma Us Inc
Firm location Birmingham, AL
Affected scope 14439 units
Distribution Nationwide, Italy, Canada, and Brazil

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

Scale of Impact

14439 units units affected - limited or regional distribution scale.

Regional (<10K units) -
Multi-state (10K – 100K units) ✓ This recall
Large-scale (100K – 1M units) -
Massive (≥1M units) -

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (F-1008-2013) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Food before acting, recall details can be updated.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
SourceCF(R) Pediatric Drops, Multivitamins with A, B, D, E and K Plus Zinc, 2 FL OZ. (60ML), NDC 66212-300-60, UPC 668212300600. Recalled by Aptalis Pharma Us Inc. Units affected: 14439 units.
Why was this product recalled?
The data suggests that the formulation does not support the shelf life of the product as labeled.
Which agency issued this recall?
This recall was issued by the FDA Food on March 6, 2013. Severity: Moderate. Recall number: F-1008-2013.
Where was the recalled product distributed?
Distribution: Nationwide, Italy, Canada, and Brazil.
What are the health risks of consuming a recalled food product?
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nationwide recalls with similar severity or category timing

Food and dietary-supplement notices outside this firm and state, matched by severity timing and product category.

Compare this recall with CCM Hockey U.S. Recalls FMHVR Hybrid Visors and ACCHVR Repl… → · All Household Products recalls

This recall: FDA Food, reported March 6, 2013. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026