RecallHawk
Class II Recall

CB1101004 BAGUETTE SUPER and CB1101005 BAGUETTE SUPER (34 u.)

GRUVIPA S.L.

Summary

The FDA issued a Class II for CB1101004 BAGUETTE SUPER and CB1101005 BAGUETTE SUPER (34 u.) by GRUVIPA S.L.. Reason: Finished product potentially adulterated with insect filth..

Details

Source

Food Recall

External ID

F-1275-2022

Action Date

2022-06-15

Status

Terminated

Category

food

Product Description

CB1101004 BAGUETTE SUPER and CB1101005 BAGUETTE SUPER (34 u.)

Lot/Code Info: LOT Best by Date 21513 Sep 11, 2022 22053 Oct 23, 2022 22055 Oct 29, 2022 22065 Nov 5, 2022 22055 Oct 25, 2022 22053 Oct 23, 2022 22125 Dec 13, 2022 22171 Jan 14, 2023 22106 Dec 4, 2022

Quantity Affected: 79,360 units

Reason for Recall

Finished product potentially adulterated with insect filth.

Distribution

Domestic distribution only (Florida).

Type: Voluntary: Firm initiated

Recall Initiated: 2022-05-23

Company

GRUVIPA S.L.

Pineda De Mar

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 197 food recalls issued in the same week, part of 204 food-related FDA actions this month.

GRUVIPA S.L. has 6 FDA actions in our database, including 6 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (GRUVIPA S.L.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does GRUVIPA S.L. have FDA actions?

GRUVIPA S.L. has 6 FDA actions in our database, including 6 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1275-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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