Cb1101001 Barra Xxl recall

Recalled by Gruvipa S.L. · Pineda De Mar, Spain

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

Why it was recalled

Finished product potentially adulterated with insect filth.

Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.

What was recalled

CB1101001 BARRA XXL

Quantity: 24,800 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.

LOT Best by Date 21512 Sep 10 2022 21514 Sep 13 2022 22054 Oct 24, 2022 22065 Nov 1, 2022 22125 Dec 16 2022 22065 Nov 11, 2022 22125 Dec 16, 2022 22171 Jan 14, 2023

Where it was sold

Florida

FDA's distribution note: Domestic distribution only (Florida).

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: Gruvipa S.L.
Initiated by: Voluntary: Firm initiated
Recall initiated: May 23, 2022
In FDA report of: Jun 15, 2022
Terminated: Aug 23, 2022
FDA recall number: F-1274-2022 · event 90287
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 Foreign material May 23, 2022