CLASS II Food recall · Reported 15 Jun 2022 · FDA Enforcement Report

Cb1115007 Silvestre Cereales recalled by Gruvipa S.l

Gruvipa S.L is recalling Cb1115007 Silvestre Cereales, distributed in Florida. The recall was initiated on 23 May 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLOT Best by Date 22053 Oct 23, 2022 22111 Dec 4, 2022
Quantity recalled7,200 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1279-2022
FDA event ID
90287
Recalling firm
Gruvipa S.L, Pineda De Mar
Classification
Class II
Status
Terminated
Recall initiated
23 May 2022
FDA classified
8 Jun 2022
Reported
15 Jun 2022
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Foreign Material
Product category
Cereal

Timeline

23 May 2022Recall initiated by company
8 Jun 2022Classified by FDA+16 days
15 Jun 2022Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Finished product potentially adulterated with insect filth.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

CB1115007 SILVESTRE CEREALES

Where it was distributed

Domestic distribution only (Florida).

Florida

Questions about this recall

Why was it recalled?

Finished product potentially adulterated with insect filth.

Which lots are affected?

LOT Best by Date 22053 Oct 23, 2022 22111 Dec 4, 2022

Where was it sold?

Domestic distribution only (Florida).

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

5 other products · FDA event 90287

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