Real Alkalized Water
Reason FDA was notified of cases of acute liver failure after consumption of Real Water
Real Alkalized Water recall
Recalled by Real Water, Inc. · Henderson, NV, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
FDA was notified of cases of acute liver failure after consumption of Real Water
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
Real Alkalized Water, packed in 16.9 oz., 1 Liter, 1.5 Liter, 1-Gallon and 5-Gallon plastic bottles. Drinkrealwater.com
Quantity: unknown
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.
Real Water 16.9 oz., UPC (Case): 6-69149-10551-1, UPC (Single): 6-69149-10550-4 Real Water 1 Liter, UPC (Case): 6-69149-10553-5, UPC (Single): 6-69149-10552-8 Real Water 1.5 Ltr, UPC (Case): 6-69149-10555-9, UPC (Single): 6-69149-10554-2 Real Water 1 Gallon, UPC (Case): 6-69149-10561-0, UPC (Single): 6-69149-10560-3 ALL CODES of all products.
Where it was sold
Nationwide.
Alabama Arizona California Colorado Georgia Illinois Minnesota Missouri Mississippi New Mexico Nevada New York Rhode Island Tennessee Washington
FDA's distribution note: Nationwide. Distributors located in WA, CA, AZ, NM, NV, RI, CO, MN, MO, IL, TN, AL, MS, GA, NY
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall.
- Recalling firm
- Real Water, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 17, 2021
- In FDA report of
- Apr 28, 2021
- FDA recall number
- F-0481-2021 · event 87552
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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