Jumbo Meat Ball Sub; Net Weight: 8.9oz; Product Code: Fresh Thru 10-15-25, 10/16/2025, 10/20/2025 In clear plastic packa
Summary
The FDA issued a Class II for Jumbo Meat Ball Sub; Net Weight: 8.9oz; Product Code: Fresh Thru 10-15-25, 10/16 by MG FOODS, INC. Reason: Mozzarella Cheese ingredient potential to be contaminated with metal shavings..
Details
Source
Food Recall
External ID
H-0083-2026
Action Date
2025-10-29
Status
Terminated
Category
food
Product Description
Jumbo Meat Ball Sub; Net Weight: 8.9oz; Product Code: Fresh Thru 10-15-25, 10/16/2025, 10/20/2025 In clear plastic packaging with white sticker label
Lot/Code Info: Fresh Thru 10-15-25, Fresh Thru 10/16/2025, Fresh Thru10/20/2025
Quantity Affected: 117 units
Reason for Recall
Mozzarella Cheese ingredient potential to be contaminated with metal shavings.
Distribution
TX, LA
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-04
Company
Longview, TX
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 91 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (MG FOODS, INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does MG FOODS, INC have FDA actions?
This is the only FDA action we have on record for MG FOODS, INC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0083-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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