SourceCF — Class II food recall F-1008-2013
Terminated recall by Aptalis Pharma Us Inc, reported 2013-03-06, distributed nationwide. The data suggests that the formulation does not support the shelf life of the product as labeled.
| Recall number | F-1008-2013 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Aptalis Pharma Us Inc, Birmingham, AL, United States |
| Recall initiated | 2013-02-04 |
| Classified | 2013-02-25 |
| Reported by FDA | 2013-03-06 |
| Terminated | 2013-07-22 |
| Distributed | Nationwide (US) |
| Countries outside the US | BR, CA, IT |
| Quantity | 14,439 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00668212300600 |
| NDC | 66212-0300-60 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-1008-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.