Cb1101001 Barra Xxl
Recalling firm: GRUVIPA S.L.
Finished product potentially adulterated with insect filth.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Aug 23, 2022.
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FDA code information
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
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Full FDA record and distribution details
Original product description
CB1101001 BARRA XXL
Original FDA recall reason
Finished product potentially adulterated with insect filth.
Recall details
- Recall number
- F-1274-2022
- Event ID
- 90287
- FDA status
- Terminated
- Initiated
- May 23, 2022
- Reported
- Jun 15, 2022
- Classified
- Jun 8, 2022
- Terminated
- Aug 23, 2022
- Quantity
- 24,800 units
- Location
- Pineda De Mar, Spain
- Initiation type
- Voluntary: Firm initiated
- Notification
- Telephone
Where it was distributed
Domestic distribution only (Florida).
Data updated September 16, 2026. View official FDA data ↗
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