Horizon Organic ORG ASEP CHOC MILK 1%
Reason Product has the potential to be spoiled.
Coconut milk recall
Recalled by Procesadora de Frutos y Vegetales del Caribe · San Cristobal, N/A, Dominican Republic (the)
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Procesadora de Frutos y Vegetales del Caribe SRL, Calle Club Rotario 24, Madre Vieja Sur, San Crist¿bal, Dominican Republic has initiated a voluntary recall due to an undeterminable number of lots of coconut milk that were thermally under processed.
These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.
What was recalled
Coconut milk , 13.5 fld oz, can, 214x406 3 pieces steel tins ,24 tins per case. Refrigerate after opening.
Quantity: 1650 cases 24/13.5fld oz
Food: Milk & dairy
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 involved are 32 ,35, 37,41,43,47,39, 53 and 57. All these lots expire on May of 2018. The UPC code that identifies the P.A Coconut milk is: 7189123232406
Where it was sold
New York
FDA's distribution note: U.S. consignees - New York, United States. No U.S. Government Agency consignees No Foreign consignees Please note: The firm ceased further distribution of the product(s) on 06/20/2015
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
- Procesadora de Frutos y Vegetales del Caribe
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 13, 2016
- In FDA report of
- Aug 24, 2016
- Terminated
- Jan 26, 2017
- FDA recall number
- F-1923-2016 · event 74670
- Official record
- FDA enforcement report search
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