FDA recall record
Penafiel Mineral Spring Water 600mL (20.3 FL OZ) and Penafiel Mineral Spring Water 1.5 L (50.7 FL OZ) packaged in clear PET bottles, 12 units per case UPC 078000200249 and 07800...
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 2, 2020. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Penafiel Mineral Spring Water 600mL (20.3 FL OZ) and Penafiel Mineral Spring Water 1.5 L (50.7 FL OZ) packaged in clear PET bottles, 12 units per case UPC 078000200249 and 078000200294
Reason
Elevated levels of inorganic arsenic
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.
Penafiel Mineral Spring Water 600mL (20.3 FL OZ) and Penafiel Mineral Spring Water 1.5 L (50.7 FL OZ) packaged in clear PET bottles, 12 units per case UPC 078000200249 and 078000200294
Code information listed by FDA
Lots : 101100619, 101100719, 101101819, 101101919, 101103319, 101103819, 101104719, 101106119, 101107519, 101109119, 102100519, 102101019, 102102119, 102102419, 102103919, 102104719, 102106319, 102106419, 102106719, 102107919, 102108019
Distribution and firm information
Recalling firm listed by FDA: Mott's LLP
Firm location listed by FDA: Plano, TX, United States
Distribution reported by FDA: Nationwide throughout the US.
Product quantity listed by FDA: 62,349 cases
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.