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
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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