Summary
The FDA issued a Class II for Norpaco GORGONZOLA STUFF OLIVE 1/7.5# SUPC/ITEM # 4481 by Greco Sidari. Reason: The food was not held at an appropriate temperature. The holding temperature could affect spoilage and potentially support pathogen growth..
Details
Source
Food Recall
External ID
F-0820-2024
Action Date
2024-02-14
Status
Terminated
Category
food
Product Description
Norpaco GORGONZOLA STUFF OLIVE 1/7.5# SUPC/ITEM # 4481
Lot/Code Info: All Lot Codes Distributed between November 26, 2023 and January 5, 2024
Quantity Affected: 1375 cases total
Reason for Recall
The food was not held at an appropriate temperature. The holding temperature could affect spoilage and potentially support pathogen growth.
Distribution
OH, NY & PA
Type: Voluntary: Firm initiated
Recall Initiated: 2024-01-11
Company
Cleveland, OH
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 82 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Greco Sidari has 36 FDA actions in our database, including 36 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 (Greco Sidari) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Greco Sidari have FDA actions?
Greco Sidari has 36 FDA actions in our database, including 36 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0820-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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