Honeyville YELLOW COLOR
Reason Undeclared Red #40.
Instant Reishi Coffee recall
Recalled by Chun Yuen Trading Co., Inc. · El Monte, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Milk is not declared on the product labeling.
Undeclared allergen: Milk
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
Instant Reishi Coffee, 4 in 1; Ca Phe Ling Chi; 20 sachets, Net Wt. 360g (12.7 oz.) UPC 8 93663 00225 8 Ingredients: Sugar, Non Dairy Creamer, Instant Coffee, Reishi Extract. Chun Yuen Trading, So. El Monte, CA
Quantity: 15,947 bags
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.
All codes: A72518 C71118 D71818 E70518 E74818 H72118 A72618 C71218 D71918 E70618 E74918 A72718 C71318 D72018 E70818 E75018 A72818 C71418 D72118 E74718 H72018
Where it was sold
Arizona California Georgia Illinois Minnesota New York Texas
FDA's distribution note: U.S. distribution to the following: GA, TX, MN, CA, AZ, TX, MN, NY, and IL. No foreign distribution.
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; 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
- Chun Yuen Trading Co., Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 25, 2017
- In FDA report of
- Nov 1, 2017
- Terminated
- May 11, 2018
- FDA recall number
- F-0034-2018 · event 78198
- Official record
- FDA enforcement report search
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