FDA recall record
Nepro Mixed Berry, 8oz metal can
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 January 31, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Nepro Mixed Berry, 8oz metal can
Reason
The firm expanded recall to include additional batches. Product recalled because of off odor and taste due to microbial contamination.
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.
Nepro Mixed Berry, 8oz metal can
Code information listed by FDA
Lot Number 59879RA00 Expiration Date 1Dec2016
Distribution and firm information
Recalling firm listed by FDA: Abbott Nutrition
Firm location listed by FDA: Altavista, VA, United States
Distribution reported by FDA: The product was distributed in the US as well as the following foreign countries: Guam and Puerto Rico, Israel, Kuwait, Trinidad and Tobago
Product quantity listed by FDA: 362,400 units
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.