FDA recall record
Probitotic Dietary Supplement. : iFlora¿ Kids Multi-Probiotic¿
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of August 20, 2013. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Probitotic Dietary Supplement. : iFlora¿ Kids Multi-Probiotic¿
Reason
On the evening of Friday, July 6, 2012, Ingredion, Inc. (f/k/a Corn Products U.S., Inc.) the supplier of Galactooligosaccharide (GOS), an ingredient included, in iFlora¿ Kids Multi Probiotic, notified our contract manufacturer that two lots of their GOS material supplied for inclusion in our products were being recalled for a suspected salmonella contamination. Although our contract manufacturer
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Probitotic Dietary Supplement. : iFlora¿ Kids Multi-Probiotic¿
Code information listed by FDA
Lot numbers: 1595811, 2089411, 1074711, 1479611, 1640811 and 1734411. UPC codes: 6 48575 01013 2 and 6 48575 01014 9 UPC Codes: 6 48575 01013 2 6 48575 01013 2 6 48575 01013 2 6 48575 01013 2
Distribution and firm information
Recalling firm listed by FDA: Nutri-Health Supplements Llc.
Firm location listed by FDA: Cottonwood, AZ, United States
Distribution reported by FDA: Distributed to retail natiowide to US states.
Product quantity listed by FDA: 4,747 bottles
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.