SourceCF (R) Pediatric Drops recall
Recalled by Aptalis Pharma Us Inc · Birmingham, AL, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
The data suggests that the formulation does not support the shelf life of the product as labeled.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What 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
Quantity: 14439 units
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
1BA67, exp Mar 13; 1DC02, exp Jun 13; 2BA86, exp Apr 14; 2FA92, exp Aug13.
Where it was sold
Nationwide.
FDA's distribution note: Nationwide, Italy, Canada, and Brazil
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Aptalis Pharma Us Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 4, 2013
- In FDA report of
- Mar 6, 2013
- Terminated
- Jul 22, 2013
- FDA recall number
- F-1008-2013 · event 64245
- Official record
- FDA enforcement report search