On cap 100% Spring Water Bottled at Aqua Filter Fresh
Reason For Spring Water and Purified Water bottled 4/17 - 18/2014, Outside lab results were positive for Coliforms non-speciated E. coli.
On cap Purified Water Bottled at Aqua Filter Fresh recall
Recalled by Aqua Filter Fresh, Inc. · Pittsburgh, PA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
For Spring Water and Purified Water bottled 4/17 - 18/2014, Outside lab results were positive for Coliforms and non-speciated E. coli.
Pathogen: E. coli
Shiga toxin-producing E. coli (such as O157:H7) can cause severe illness and kidney failure.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
On cap Purified Water Bottled at Aqua Filter Fresh, Inc., Pittsburgh, PA 15239 Permit #504 Source: Plum Boro Municipal Authority 15239 Processed by Reverse Osmosis, Steam Distillation, Micro-filtration, Ozonation, UV *Minerals added for taste On Bottle side: Tyler Mountain Water & Coffee In 4 gallon and 5 gallon plastic bottles
Quantity: 2436 bottles
Food: Fresh fruit 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.
MFG 041714 EXP 041715 MFG 041814 EXP 041815
Where it was sold
Pennsylvania West Virginia
FDA's distribution note: PA, WV
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
- Aqua Filter Fresh, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 23, 2014
- In FDA report of
- May 28, 2014
- Terminated
- Nov 4, 2015
- FDA recall number
- F-1950-2014 · event 68202
- 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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