Summary
The FDA issued a Class II for CB1102052 BOCATA ESPECIAL CASERO'S by GRUVIPA S.L.. Reason: Finished product potentially adulterated with insect filth..
Details
Source
Food Recall
External ID
F-1278-2022
Action Date
2022-06-15
Status
Terminated
Category
food
Product Description
CB1102052 BOCATA ESPECIAL CASERO'S
Lot/Code Info: LOT Best By Date 21443 Jul 24, 2022 21493 Aug 28, 2022 21494 Aug 29, 2022 21511 Sep 9, 2022 21511 Sep 9, 2022 22043 Oct 16, 2022 22044 Oct 17, 2022 22045 Oct 18, 2022 22052 Oct 22, 2022 22054 Oct 24, 2022 22043 Oct 16, 2022 22044 Oct 17, 2022 22052 Oct 22, 2022 22054 Oct 24, 2022 22063 Oct 30, 2022 22064 Oct 31, 2022 22065 Nov 1, 2022 22065 Nov 1, 2022 22073 Nov 6, 2022 22075 Nov 8, 2022 22081 Nov 8, 2022 22084 Nov 14, 2022 22085 Nov 15, 2022 22093 Nov 20, 2022 22094 Nov 22, 2022 22094 Nov 21, 2022 22124 Dec 12, 2022 22125 Dec 16, 2022 22126 Dec 16, 2022 22126 Dec 16, 2022 22142 Dec 24, 2022 22144 Dec 26, 2022 22152 Dec 31, 2022 22153 Jan 1 2023 22161 Jan 6, 2023 22162 Jan 7, 2023
Quantity Affected: 116,160 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-1278-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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