Summary
The FDA issued a Class I for B57820 BREADER X1 50.00 BAG by Newly Weds Foods, Inc.. Reason: Products may contain Salmonella.
Details
Source
Food Recall
External ID
F-1091-2023
Action Date
2023-07-12
Status
Terminated
Category
food
Product Description
B57820 BREADER X1 50.00 BAG
Lot/Code Info: MT110322L MT110822M
Quantity Affected: 6,465,115.78 pounds Total
Reason for Recall
Products may contain Salmonella
Distribution
ALABAMA, ARKANSAS, CALIFORNIA, COLORADO, FLORIDA, GEORGIA, ILLINOIS, INDIANA, IOWA, KANSAS, KENTUCKY, LOUISIANA, MICHIGAN, MINNESOTA, MISSISSIPPI, MISSOURI, MONTANA, NEBRASKA, NEW JERSEY, NEW YORK, NORTH CAROLINA, OHIO, OKLAHOMA, OREGON, PENNSYLVANIA, TENNESSEE, TEXAS ,WISCONSIN. CANADA.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-05-26
Company
Chicago, IL
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 228 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Newly Weds Foods, Inc. has 221 FDA actions in our database, including 221 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 (Newly Weds 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 Newly Weds Foods, Inc. have FDA actions?
Newly Weds Foods, Inc. has 221 FDA actions in our database, including 221 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1091-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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