Penafiel Mineral Spring Water 600mL (20.3 FL OZ) and Penafiel Mineral Spring Water 1.5 L (50.7…
Recalling firm: Mott's LLP
Elevated levels of inorganic arsenic
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jan 2, 2020.
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078000200249FDA code information
Lots : 101100619, 101100719, 101101819, 101101919, 101103319, 101103819, 101104719, 101106119, 101107519, 101109119, 102100519, 102101019, 102102119, 102102419, 102103919, 102104719, 102106319, 102106419, 102106719, 102107919, 102108019
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Full FDA record and distribution details
Original product description
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
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 078000200249 | g Water 1.5 L (50.7 FL OZ) packaged in clear PET bottles, 12 units per case UPC 078000200249 and 078000200294 |
Original FDA recall reason
Elevated levels of inorganic arsenic
Recall details
- Recall number
- F-1971-2019
- Event ID
- 83145
- FDA status
- Terminated
- Initiated
- Jun 18, 2019
- Reported
- Aug 14, 2019
- Classified
- Aug 6, 2019
- Terminated
- Jan 2, 2020
- Quantity
- 62,349 cases
- Location
- Plano, TX, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
Nationwide throughout the US.
Data updated September 16, 2026. View official FDA data ↗
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