Horizon Organic ORG ASEP CHOC MILK 1%
Reason Product has the potential to be spoiled.
Chocolate Cream Pie recall
Recalled by 3 Fellers · Goochland, VA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Chocolate pie contains almonds which are not declared on the label.
Undeclared allergen: Tree nuts
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Chocolate Cream Pie, 4.5 oz. package, 12 pks/case. UPC # 891796002732
Quantity: 3480 units
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.
Sell by dates: 10/29/2013 11/8/2013 12/13/2013 1/3/2014 2/19/2014 3/12/2014 3/17/2014 3/30/2014 4/24/2014 4/29/2014 5/6/2014 5/7/2014
Where it was sold
California District of Columbia Delaware Kentucky Maryland New Jersey Ohio Pennsylvania Virginia
FDA's distribution note: Products were distributed in Southern California, Virginia, Maryland, District of Columbia, Delaware, Pennsylvania, New Jersey, Ohio, and Kentucky.
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. The risk from an undeclared allergen is to people allergic to tree nuts; for anyone else the product is generally not a safety concern. 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
- 3 Fellers
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 7, 2013
- In FDA report of
- Dec 25, 2013
- Terminated
- Mar 24, 2014
- FDA recall number
- F-1111-2014 · event 66932
- Official record
- FDA enforcement report search
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