Class IITerminated in FDA datasetJan 19, 2018

IQF blend product sold as Not Ready To Eat (NRTE) product for use in foodservice or manufacturing applications. The product cases are labeled with instructions to cook product. -Monarch…

Recalling firm: National Frozen Foods Corporation--Seattle

Why it was recalled

Frozen blend vegetable product containing green beans are recalled due to a potential contamination with Listeria monocytogenes.

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Compare the exact product and package details with the label you have.

ProductIQF blend product sold as Not Ready To Eat (NRTE) product for use in foodservice or manufacturing applications. The product cases are labeled with instructions to cook product. -Monarch brand, IQF frozen Capri Vegetable Blend, Ingredients: Carrots, Green Beans, Yellow Squash, and Zucchini. NFFC item #58108-00602, UPC #670229, packaged in 20 lbs. case. -Simplot Classic, IQF frozen Meadow Blend, Ingredients: Carrots, Green Beans, Zucchini, Yellow Squash. NFFC item #71179-67166, no UPC, packaged in a 2 lbs. bags, 12 bags per case.

FDA code information

Monarch brand lot # 38511-7H11G3N and 38511-7H11H3N. Simplot Classic lot # 965AUG081705H.

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Full FDA record and distribution details

Original product description

IQF blend product sold as Not Ready To Eat (NRTE) product for use in foodservice or manufacturing applications. The product cases are labeled with instructions to cook product. -Monarch brand, IQF frozen Capri Vegetable Blend, Ingredients: Carrots, Green Beans, Yellow Squash, and Zucchini. NFFC item #58108-00602, UPC #670229, packaged in 20 lbs. case. -Simplot Classic, IQF frozen Meadow Blend, Ingredients: Carrots, Green Beans, Zucchini, Yellow Squash. NFFC item #71179-67166, no UPC, packaged in a 2 lbs. bags, 12 bags per case.

Recall details

Recall number
F-0825-2018
Event ID
78988
FDA status
Terminated
Initiated
Jan 19, 2018
Reported
Feb 28, 2018
Classified
Feb 20, 2018
Terminated
May 15, 2018
Quantity
2,814 cases of mixed vegetables.
Location
Seattle, WA, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

distributed in AK, AR, AZ, CA, CO, FL, ID, IL, KS, MI, MS, MT, ND, NE, NM, NV, OR, TN, TX, VA, and WA.

FDA source record · F-0825-2018

Data updated September 16, 2026. View official FDA data ↗

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