Baklava
Reason Undeclared Soybean oil
Biscotti-Plain recall
Recalled by Paximadi Co. LLC · Seattle, WA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Biscotti- Plain product is recalled because the ingredients statement on the master bulk case label declared butter but it does not declare milk.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
Biscotti-Plain. Product is bulk packed in a master cardboard case and each master case contains either 48 or 36 individual biscotti. There are 12 Biscotti per layer and separated between layers with wax paper. Label applied to the exterior of master case only. The master case's label is read in parts: "***Paximadi Co***Biscotti-Plain***Unbleached Enriched Flour (Wheat Flour, Malted Barley Flour, Niacin, Thiamine, Mononitrate, Riboflavin, Folic Acid), Natural Sugar, Vanilla (Dextrose, Cornstarch, Vanilla Bean Extracts, Artificial Flavor), Baking Soda, Salt, Eggs, Butter (Pasteurized Cream and Salt), Olive Oil, Almonds***Net Wt 1oz Each***.
Quantity: 84 pieces
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.
No codes on individual product. The delivery date of 4/24 marked on the master boxes.
Where it was sold
Washington
FDA's distribution note: distributed in WA.
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. 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
- Paximadi Co. LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 30, 2019
- In FDA report of
- Jun 5, 2019
- Terminated
- Jun 27, 2019
- FDA recall number
- F-1423-2019 · event 82747
- Official record
- FDA enforcement report search