Panang Curry included in the Beef Panang Curry Dinner recall
Recalled by Good Eggs SF - Bay · San Francisco, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Panang Curry included in the Beef Panang Curry Dinner does not list peanuts as an allergen, although peanuts are listed as an ingredient.
Undeclared allergen: Peanut
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
Panang Curry included in the Beef Panang Curry Dinner, 3.5 oz. 8oz plastic deli container bearing the name Curry Paste. Ingredients: Shallots, Ginger, Garlic, Peanuts, Sugar, Tomato Paste, Fish Sauce(Anchovies, water, salt), Serrano Chili, Tumeric, Galangal, Lemon grass Cumin, Coriander, Kefir Lime Leaf, Shrimp Powder, Contains: Fish Crustaceans, Shellfish Keep Refrigerated
Quantity: 547 containers
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.
Use by September 8, 2017
Where it was sold
California
FDA's distribution note: Direct customers in Bay Area of CA only.
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 peanut; 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
- Good Eggs SF - Bay
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 7, 2017
- In FDA report of
- Oct 11, 2017
- Terminated
- Nov 2, 2017
- FDA recall number
- F-0010-2018 · event 78095
- Official record
- FDA enforcement report search