Superbudin
Reason Undeclared allergens: wheat. and soy One of the ingredients is "Super Pan" that contains wheat as a sub-ingredient. The coconut milk is another ingredient that contains "soy lecithin" and it is undeclared.
SUPERPAN***Tu Pan Natural recall
Recalled by Lucy's Kitchen, Inc. · San Juan, PR, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Undeclared allergens: wheat. The list of ingredients declare "semolina durum" but not the common name "wheat".
Undeclared allergen: Wheat
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
"***SUPERPAN***Tu Pan Natural***"
Quantity: 6985 units
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.
3107291300, 3107301300, 3107311300, 3108011300, 3108031300, 3208051300, 3208061300, 3208971300, 3208081300, 3208091300
Where it was sold
Puerto Rico
FDA's distribution note: PR only
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to wheat; 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
- Lucy's Kitchen, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 20, 2013
- In FDA report of
- Sep 25, 2013
- Terminated
- Apr 26, 2017
- FDA recall number
- F-1893-2013 · event 65983
- 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.