Poco Dolce Bittersweet Chocolate recall

Recalled by Poco Dolce Confections, Inc. · San Francisco, CA, United States

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

Why it was recalled

California Department of Public Health conducted and inspection of the firm and found that milk was missing from the label as an ingredient of butter.

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

Poco Dolce Bittersweet Chocolate: Burnt Caramel Tile, sea salt topped; 0.6 oz (17 grams) San Francisco CA. Ingredients: Bittersweet Chocolate (Chocolate Liquor, Sugar, Cocoa Butter, Soy Lecithin, Pure Vanilla) Sugar, Butter, Grey Sea Salt. May contain traces of peanuts, tree nuts or milk proteins.

Quantity: 34, 641 individual atile, all varieties

Food: Chocolate & candy

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

Where it was sold

Arizona California Colorado Connecticut District of Columbia Florida Georgia Illinois Massachusetts Maryland Michigan New Jersey New Mexico New York Oregon Pennsylvania Utah Washington

FDA's distribution note: CA, AZ, CO. CT, DC, FL, GA, IL, MA, MD, MD, MI, NJ, NM, NY, OR, PA, UT and 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: Poco Dolce Confections, Inc.
Initiated by: Voluntary: Firm initiated
Recall initiated: May 1, 2015
In FDA report of: May 20, 2015
Terminated: Jul 23, 2015
FDA recall number: F-2250-2015 · event 71144
Official record: FDA enforcement report search

Also recalled with it (5 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Terminated Labeling May 1, 2015