Daisy s Bakery Inc recall
Recalled by Daisy's Bakery Inc. · Clifton, NJ, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Daisy s Bakery Inc. has decided to recall Gourmet Concha, 4 oz., because the product is mis-labeled and has an undeclared milk allergen.
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
Daisy s Bakery Inc., Gourmet Concha, 4 oz. / 1 per package, Plastic Bag, 12 units per case
Quantity: 590 one dozen boxes
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.
441, 442, 443, 444, 445, 446, 447, 448, 449, 450, 451, 452, 453, 454, 455, 456, 457, 458, 459, 460, 461, 462, 463, 464, 465, 466, 467, 468, 469, 470, 471
Where it was sold
Florida Illinois North Carolina New Jersey New York
FDA's distribution note: The product was distributed to the following states New York, New Jersey, Florida, Illinois and North Carolina .
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
- Daisy's Bakery Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 22, 2017
- In FDA report of
- Jan 17, 2018
- Terminated
- Jun 13, 2018
- FDA recall number
- F-0565-2018 · event 78831
- Official record
- FDA enforcement report search