Macaroni & Cheese, Macarrones con Queso; 3-5 lb pouches/bolsas, NET WT/PESO NETO 240 OZ (15 LB) 6.80 kg; distributed by
Summary
The FDA issued a Class I for Macaroni & Cheese, Macarrones con Queso; 3-5 lb pouches/bolsas, NET WT/PESO NETO by Sandridge Food Corporation. Reason: Undeclared Egg Allergen.
Details
Source
Food Recall
External ID
F-0503-2022
Action Date
2022-01-12
Status
Terminated
Category
food
Product Description
Macaroni & Cheese, Macarrones con Queso; 3-5 lb pouches/bolsas, NET WT/PESO NETO 240 OZ (15 LB) 6.80 kg; distributed by Gordon Food Service, Reorder No. 540061, Vendor Item # 4357505, Perishable. Keep Refrigerated. Perecedero. Mantener Refrigerado.
Lot/Code Info: Best By 01/11/2022
Quantity Affected: 24 cases
Reason for Recall
Undeclared Egg Allergen
Distribution
Product was shipped to a Gordon Food Service in Texas. Gordon Food Service then distributed it to 3 restaurants and a hotel.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-12-27
Company
Medina, OH
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 11 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 (Sandridge Food Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Sandridge Food Corporation have FDA actions?
This is the only FDA action we have on record for Sandridge Food Corporation in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0503-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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