FDA recall record
CB1101001 BARRA XXL
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of August 23, 2022. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
CB1101001 BARRA XXL
Reason
Finished product potentially adulterated with insect filth.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
CB1101001 BARRA XXL
Code information listed by FDA
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
Distribution and firm information
Recalling firm listed by FDA: GRUVIPA S.L.
Firm location listed by FDA: Pineda De Mar, Spain
Distribution reported by FDA: Domestic distribution only (Florida).
Product quantity listed by FDA: 24,800 units
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.