Seafood Ball Combo Assorti Boulettes Aux Products De Mer Fish Ball
Reason Canadian Food Inspection Agency analytical results revealed the presence of undeclared egg allergen.
Fried Shrimp Flavoured Fish Bar recall
Recalled by Way Fong LLC · Maspeth, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Canadian Food Inspection Agency analytical results revealed the presence of undeclared egg allergen.
Undeclared allergen: 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
FRIED SHRIMP FLAVOURED FISH BAR, Net Wt 9.07 Kg 4 X 5 lbs. bulk, Product of Canada, KEEP REFRIGERATED
Quantity: 15 cases
Food: Seafood & fish
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 lot numbers beginning with "0" and "8"
Where it was sold
New York
FDA's distribution note: New York
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 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
- Way Fong LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 16, 2016
- In FDA report of
- Jul 13, 2016
- Terminated
- May 8, 2017
- FDA recall number
- F-1629-2016 · event 73713
- 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.
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