Bulk, frozen french fries as Shoestring 1/4" Frozen Grade A Fancy Fry packed in clear poly bag with lot code "200 APR 17
Summary
The FDA issued a Class I for Bulk, frozen french fries as Shoestring 1/4" Frozen Grade A Fancy Fry packed in by JR Simplot Food Group. Reason: Frozen french fries is being recalled due to undeclared wheat..
Details
Source
Food Recall
External ID
F-1320-2022
Action Date
2022-06-29
Status
Terminated
Category
food
Product Description
Bulk, frozen french fries as Shoestring 1/4" Frozen Grade A Fancy Fry packed in clear poly bag with lot code "200 APR 17 22" and packed in cardboard case that is labeled in part, "Bountiful HARVEST***ORIGINALS SHOESTRING 1/4" FROZEN GRADE A FANCY FRY NO ARTIFICIAL FLAVORS OR COLORS 22924 1630***60822486229247***6-4.5 LB. BAGS NET WT. 27 LBS. (12.2 kg)***200 APR 17 22***INGREDIENTS: POTATOES, VEGETABLE OIL (SOYBEAN, CANOLA, AND/OR COTTONSEED OILS), CONTAINS LESS THAN 2% OF DEXTROSE, DISODIUM DIHYDROGEN PYROPHOSPHATE (TO MAINTAIN NATURAL COLOR)."
Lot/Code Info: Item no. 60822486229247 Lot Code: 200 APR 17 22 Breakdown: "200" Production Facility; "APR" Production Month; "17" Production Date; "22" Production Year
Quantity Affected: 3207 cases
Reason for Recall
Frozen french fries is being recalled due to undeclared wheat.
Distribution
Product was distributed wholesale as a food service item to distributors in CO, AZ, NM, CA, IA, PA, TN, LA, WI, MN, AL and WA.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-06-07
Company
Boise, ID
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 78 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 (JR Simplot Food Group) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does JR Simplot Food Group have FDA actions?
This is the only FDA action we have on record for JR Simplot Food Group in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1320-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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