Mineral Spring Water (Penafiel) – Arsenic Levels (2019)
Class III: A situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences
Class III recall indicates unlikely adverse health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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
Brand
Mott's LLP
Lot Codes / Batch Numbers
Lots : 101100619, 101100719, 101101819, 101101919, 101103319, 101103819, 101104719, 101106119, 101107519, 101109119, 102100519, 102101019, 102102119, 102102419, 102103919, 102104719, 102106319, 102106419, 102106719, 102107919, 102108019
Products Sold
Lots : 101100619, 101100719, 101101819, 101101919, 101103319, 101103819, 101104719, 101106119, 101107519, 101109119, 102100519, 102101019, 102102119, 102102419, 102103919, 102104719, 102106319, 102106419, 102106719, 102107919, 102108019
Mott's LLP is recalling Penafiel Mineral Spring Water 600mL (20.3 FL OZ) and Penafiel Mineral Spring Water 1.5 L (50.7 FL OZ due to Elevated levels of inorganic arsenic. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Elevated levels of inorganic arsenic
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 6, 2026