Member's Mark brand BREADED MOZZARELLA STICKS; 72 STICKS; 2 RESEALABLE BAGS INCLUDED; NET WT 5 LB (2.26 kg); UPC 0787422
Summary
The FDA issued a Class I for Member's Mark brand BREADED MOZZARELLA STICKS; 72 STICKS; 2 RESEALABLE BAGS INCL by Rich Products Corp. Reason: Product contains undeclared egg and soy..
Details
Source
Food Recall
External ID
F-1380-2023
Action Date
2023-08-16
Status
Terminated
Category
food
Product Description
Member's Mark brand BREADED MOZZARELLA STICKS; 72 STICKS; 2 RESEALABLE BAGS INCLUDED; NET WT 5 LB (2.26 kg); UPC 078742226880
Lot/Code Info: Product Code 22688; Best By 12/28/2024
Quantity Affected: 15 Cases
Reason for Recall
Product contains undeclared egg and soy.
Distribution
OH, KY, PA, VA, WV
Type: Voluntary: Firm initiated
Recall Initiated: 2023-07-24
Company
Buffalo, NY
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 102 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Rich Products Corp has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Rich Products Corp) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Rich Products Corp have FDA actions?
Rich Products Corp has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1380-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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