Honeyville YELLOW COLOR
Reason Undeclared Red #40.
Penafiel Mineral Spring Water recall
Recalled by Mott's LLP · Plano, TX, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Elevated levels of inorganic arsenic
Some of these cause harm only with repeated exposure (lead in spices, for example), others act within hours (histamine poisoning from spoiled fish). All chemical contamination recalls.
What was recalled
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
Quantity: 62,349 cases
Food: Juice & beverages
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.
Lots : 101100619, 101100719, 101101819, 101101919, 101103319, 101103819, 101104719, 101106119, 101107519, 101109119, 102100519, 102101019, 102102119, 102102419, 102103919, 102104719, 102106319, 102106419, 102106719, 102107919, 102108019
Where it was sold
Nationwide.
FDA's distribution note: Nationwide throughout the US.
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. 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
- Mott's LLP
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 18, 2019
- In FDA report of
- Aug 14, 2019
- Terminated
- Jan 2, 2020
- FDA recall number
- F-1971-2019 · event 83145
- Official record
- FDA enforcement report search
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