Severity
Moderate
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.
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 FDA Food action (record #F-1008-2013) was formally reported on March 6, 2013, with the manufacturer initiating the action on February 4, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Aptalis Pharma Us Inc is listed as the recalling firm, operating out of Birmingham, AL. Federal records list the affected scope as 14439 units.
The documented reason for this recall is: The data suggests that the formulation does not support the shelf life of the product as labeled. Distribution data in the federal record shows the product reached: Nationwide, Italy, Canada, and Brazil. Distribution scope 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 - 3,056 household products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. 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.
Affected scope
14439 units
Related Recalls
6
0 from same agency
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
| 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.
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.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1008-2013) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
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.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported March 6, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.