Flathau's Fine Foods Cheese Straws Delta Bred Cheese Straws packaged in 4oz and 6oz cartons 12 packages per case
Summary
The FDA issued a Class II for Flathau's Fine Foods Cheese Straws Delta Bred Cheese Straws packaged in 4oz and by Flathau's Fine Foods. Reason: Undeclared Allergens - Wheat & Milk.
Details
Source
Food Recall
External ID
F-0044-2023
Action Date
2022-10-26
Status
Terminated
Category
food
Product Description
Flathau's Fine Foods Cheese Straws Delta Bred Cheese Straws packaged in 4oz and 6oz cartons 12 packages per case
Lot/Code Info: Batch Numbers: 33122C, 6222C, 8422C Product Numbers: 7711, DL2 Best By: 12-31-22, 03/02/23, 05/24/23
Quantity Affected: 433 total
Reason for Recall
Undeclared Allergens - Wheat & Milk
Distribution
Products were distributed in the following states: AL, AR, LA, MS, NV, NM, NC, PA, SC, TN, TX, and WA.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-09-15
Company
Petal, MS
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 41 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 (Flathau's Fine Foods) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Flathau's Fine Foods have FDA actions?
This is the only FDA action we have on record for Flathau's Fine Foods in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0044-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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