Chef s Request professional steak marinade and Buckhead wildlife marinade recall
Recalled by Deli Star Ventures Inc. dba King's Food Products · Belleville, IL, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Deli Star Inc. dba King's Food Products initiated a voluntary recall of Chef s Request professional steak marinade and Buckhead wildlife marinade due to undeclared allergens soy and wheat.
Undeclared allergens: Soy Wheat
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Chef s Request professional steak marinade and Buckhead wildlife marinade, 12oz, 64oz, 1 gallon; shelf stable, refrigerate after opening
Quantity: 4,715lbs. of buckead and 4,088.5lbs of chefs request
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Chef s request internal item number 13255 Buckhead internal item number 13259 Production Date/Production lot Code 7-26-18 82071 2-16-18 80471 1-18-18 80181 10-2-17 72751 7-18-17 71991 7-17-17 71981 1-20-17 70201
Where it was sold
Illinois Virginia
FDA's distribution note: Domestic: Illinois Foreign/VA/DOD: None
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to soy, wheat; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Deli Star Ventures Inc. dba King's Food Products
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 9, 2018
- In FDA report of
- Nov 21, 2018
- Terminated
- Feb 7, 2019
- FDA recall number
- F-0619-2019 · event 80835
- Official record
- FDA enforcement report search