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FDA source record Class I Terminated

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. Th...

Recall Date: 2023-03-30 Recalling Firm: Lamb Weston Sales Record Ref: F-0749-2023

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns 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. Th... and names Lamb Weston Sales as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Lamb Weston Sales
  • Classification: Class I
  • Status: Terminated
  • Recall date: 2023-03-30
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Product Description & Identification

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).

Reason for Recall / Hazard Identified

Undeclared Wheat in foodservice item Hashbrown patties.

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

Distributed in CA, IA, IL, KS, LA MO, MS, NM, TN, UT, VA and in Panama, Philippines, and Vietnam.

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-0749-2023
Indexed update
2026-08-09 21:59:13 UTC
Official source
Open issuing-agency record