G5300 Lamb's Supreme Hash Brown Patties, Frozen, 24 patties packed in blank unlabeled tray, 12 trays packaged in one cas
Summary
The FDA issued a Class I for G5300 Lamb's Supreme Hash Brown Patties, Frozen, 24 patties packed in blank unla by Lamb Weston Sales. Reason: Undeclared Wheat in foodservice item Hashbrown patties..
Details
Source
Food Recall
External ID
F-0749-2023
Action Date
2023-05-03
Status
Terminated
Category
food
Product Description
G5300 Lamb's Supreme Hash Brown Patties, Frozen, 24 patties packed in blank unlabeled tray, 12 trays packaged in one case. Net Wt. 33.75LB (15.30kg). UPC 1 00 44979 75300 7. The ingredients statement read: POTATOES, VEGETABLE OIL (CONTAINS OR OR MORE OF THE FOLLOWING: CANOLA, PALM, SOYBEAN, SUNFLOWER), SALT, DEHYDRATED POTATO, DEXTROSE, DISODIUM DIHYDROGEN PYROPHOSPHATE (TO MAINTAIN COLOR).
Lot/Code Info: 6050 03 04 25 21 16:06 P:2023.03.04 E:2025.03.04 6050 03 05 25 21 00:01 P:2023.03.05 E:2025.03.05 P: Year, month, day (Production date): March 4, 2023 and March 5, 2023. E: Year, month, day (Expiration data): March 4, 2025 and March 5, 2025. 6050 = Plant code for Richland Plant. 03 = Month 04 = Day 21 = Line manufactured and packed on 16:06= Time stamp
Quantity Affected: 1605 cases
Reason for Recall
Undeclared Wheat in foodservice item Hashbrown patties.
Distribution
Distributed in CA, IA, IL, KS, LA MO, MS, NM, TN, UT, VA and in Panama, Philippines, and Vietnam.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-03-30
Company
Kennewick, WA
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 28 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lamb Weston Sales has 4 FDA actions in our database, including 4 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 (Lamb Weston Sales) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lamb Weston Sales have FDA actions?
Lamb Weston Sales has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0749-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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