Food Recall Check
Class II · Moderate risk Ongoing Initiated Jan 20, 2016 (11 years ago)

Fruit Tartlets lemon flavor recall

Recalled by Ouhlala Gourmet Llc · Coral Gables, FL, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Products contain undeclared milk on finished product labeling

Undeclared allergen: Milk

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

Fruit Tartlets, lemon flavor, 9 - 0.53oz (15 g) tartlets - Net Wt. 4.8 oz (135 g). Manufactured in France. Distributed by Ouhlala Gourmet Corp. dba Buddy Fruits, Coral Gables, FL

Quantity: 9,159 12-ct cases

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.

Lot Code (Exp date): 08192016 (08192016), 09292016 (09292016), 10092015 (10092015), 10302016 (10302016), 10312016 (10312016), 111216 (111216), 10012016 (10012016), 09292016 (09292016), 10312016 (10312016). Item GTIN #00810387020566. Case UPC #20854417002430.

Where it was sold

Nationwide.

FDA's distribution note: Product distributed nationwide an internationally to the following countries: Egypt, Bermuda, and United Arab Emirates

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 milk; for anyone else the product is generally not a safety concern.

Recalling firm
Ouhlala Gourmet Llc
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 20, 2016
In FDA report of
Jun 8, 2016
FDA recall number
F-1419-2016 · event 73670
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.