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RECALL RECORD — CLASS IIRecall closedF-1274-2022/FDA enforcement
Gruvipa S.l.·Food·May 23, 2022

CB1101001 Barra Xxl

What you need to know

Class II

  • What happened

    Finished product potentially adulterated with insect filth.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. An unlabeled prescription or controlled substance was found in a product sold as food or a supplement.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDADistribution not listedMore food

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Product identification

Source: FDA FOOD

Brand nameGruvipa S.l.
Recalling firmGruvipa S.l.Pineda De Mar, Spain
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • 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 area

Domestic distribution only (Florida).

United States

Quantity affected24, 800 units
Recall initiationFDA report date: June 15, 2022
FDA recall numberF-1274-2022

Beyond the headline

The recall, in context

Gruvipa S.l. initiated this food recall on May 23, 2022. The FDA enforcement report states: Finished product potentially adulterated with insect filth. The FDA report lists distribution as: Domestic distribution only (Florida).

The FDA enforcement report describes the reason as: Finished product potentially adulterated with insect filth.

CB1101001 Barra Xxl was made or distributed by Gruvipa S.l. in Pineda De Mar, Spain. This page reflects FDA report F-1274-2022, dated June 15, 2022.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, an unlabeled prescription or controlled substance was found in a product sold as food or a supplement.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the CB1101001 Barra Xxl recall?

Gruvipa S.l. recalled CB1101001 Barra Xxl in an FDA Class II enforcement action reported as F-1274-2022. Finished product potentially adulterated with insect filth.

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Gruvipa S.l. recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1274-2022. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by Gruvipa S.l.

View brand
Class II·

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Finished product potentially adulterated with insect filth.

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Class II·

Gruvipa S.l.

CB1101006 Barra Larga Con Salvado

Finished product potentially adulterated with insect filth.

Distribution not listedFood

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.