Back to Nature Cheddalicious Cheese Flavored Crackers 6 oz.. UPC: 8-19898-01491-0 6 cartons per case
Summary
The FDA issued a Class I for Back to Nature Cheddalicious Cheese Flavored Crackers 6 oz.. UPC: 8-19898-01491- by B&G Foods North America, Inc. Reason: Undeclared egg and milk due to mispackaging.
Details
Source
Food Recall
External ID
F-1005-2022
Action Date
2022-04-20
Status
Terminated
Category
food
Product Description
Back to Nature Cheddalicious Cheese Flavored Crackers 6 oz.. UPC: 8-19898-01491-0 6 cartons per case
Lot/Code Info: SEP 05 2022
Quantity Affected: 1855 cases
Reason for Recall
Undeclared egg and milk due to mispackaging
Distribution
Distributed to distributor in CA, WI, NY, NJ, CO, IN, ME, GA, and CT
Type: Voluntary: Firm initiated
Recall Initiated: 2022-04-01
Company
Parsippany, NJ
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 40 food recalls issued in the same week, part of 204 food-related FDA actions this month.
B&G Foods North America, Inc has 3 FDA actions in our database, including 3 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 (B&G Foods North America, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does B&G Foods North America, Inc have FDA actions?
B&G Foods North America, Inc has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1005-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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