BURGER BUN WITH SEEDS 3507402 Flour, water, potato flour, eggs, sugar, shortening, milk powder, salt, yeast, S200 UPC 68
Summary
The FDA issued a Class I for BURGER BUN WITH SEEDS 3507402 Flour, water, potato flour, eggs, sugar, shortenin by Saffron Inc.. Reason: The firm was notified that their labels do not list the allergens wheat and sesame..
Details
Source
Food Recall
External ID
F-1399-2023
Action Date
2023-08-16
Status
Ongoing
Category
food
Product Description
BURGER BUN WITH SEEDS 3507402 Flour, water, potato flour, eggs, sugar, shortening, milk powder, salt, yeast, S200 UPC 682863 049657
Lot/Code Info: All codes up to and including Sell By SEPT 29 23
Quantity Affected: 384cs/10 bags/6ct buns
Reason for Recall
The firm was notified that their labels do not list the allergens wheat and sesame.
Distribution
Product was shipped to one distributor in South Carolina.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-06-30
Company
North Charleston, SC
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.
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 (Saffron Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Saffron Inc. have FDA actions?
This is the only FDA action we have on record for Saffron Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1399-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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