Horizon Organic ORG ASEP CHOC MILK 1%
Reason Product has the potential to be spoiled.
Farmer's All Natural 2% Reduced Fat Chocolate Milk recall
Recalled by Royal Crest Dairy, Incorporated · Longmont, CO, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Potential Egg Allergen contamination of Chocolate Milk.
Undeclared allergens: Milk Egg
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
Farmer's All Natural 2% Reduced Fat Chocolate Milk, One Pint (473 mL), Packaged in food safe, single-trip, polyethylene plastic bottles. UPC Code: 8 33066 00895 2. Royal Crest Dairy www.royalcrestdairy.com Plant # 08-66-Longmont Colorado. Distributed by: RCD, Inc. Denver, Colorado. Keep refrigerated under 40¿F for best shelf life. Note: 20 bottles/case.
Quantity: 8 cases (20 units) and 2 units = 162 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.
Plant # 08-66 Lot # 08222022 Best By Date: AUG 22 (08-22-2022)
Where it was sold
Colorado
FDA's distribution note: Southern Colorado.
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 milk, egg; 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
- Royal Crest Dairy, Incorporated
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 2, 2022
- In FDA report of
- Sep 28, 2022
- Terminated
- Jan 18, 2023
- FDA recall number
- F-1745-2022 · event 90713
- Official record
- FDA enforcement report search
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