Potato & Mushroom Dumplings
Reason The product contains undeclared milk and soy based on observations found during a joint inspection by the FDA and New York State Department of Agriculture & Markets.
Potato Dumplings Net Weight recall
Recalled by Js Pelmeni Ok, Inc. · Brooklyn, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
The product contains undeclared milk and soy based on observations found during a joint inspection by the FDA and New York State Department of Agriculture & Markets.
Undeclared allergens: Milk Soy
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
Potato Dumplings, Net Weight 2 lb. (32 oz.), KEEP FROZEN, UPC 6 54368 10038 6, EST # A613069 --- JS Pelmeni OK - 667 Coney Island Ave., Brooklyn, NY 11218 - (718) 469-1490
Quantity: N/A
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.
UPC 6 54368 10038 6 and no other coding
Where it was sold
Illinois Massachusetts New Jersey New York Pennsylvania
FDA's distribution note: New York, Massachusetts, Pennsylvania, New Jersey, and Illinois.
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, soy; 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
- Js Pelmeni Ok, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 13, 2013
- In FDA report of
- Mar 6, 2013
- Terminated
- May 22, 2018
- FDA recall number
- F-1029-2013 · event 64360
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.