CB1101001 BARRA XXL — FDA record F-1274-2022

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date May 23, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
CB1101001 BARRA XXL
Reason
Finished product potentially adulterated with insect filth.
Classification
Class II
Recalling firm
GRUVIPA S.L.
Quantity
24,800 units
Agency-reported status
Terminated
Source record identifier
F-1274-2022

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityLOT 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

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

Domestic distribution only (Florida).

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Jun 15, 2022
Recall initiation date
May 23, 2022
Center classification date
Jun 8, 2022
Termination date
Aug 23, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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