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FDA recall record

Italian Vegetable Blend. Product is frozen, not ready to eat, label carries cooking instruction. Label reads in part "***GARDEN FRESH***64775***47374***ITALIAN BLEND CON...

Recall F-0208-2016Class IITerminatedJuly 15, 2015

FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.

FDA listed a termination date of January 29, 2016. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

Italian Vegetable Blend. Product is frozen, not ready to eat, label carries cooking instruction. Label reads in part "***GARDEN FRESH***64775***47374***ITALIAN BLEND CONTAINS: ZUCCHINI, CARROTS, CAULIFLOWER, LIMAS, ITALIAN BEANS***20 LB NET WT***" No UPC on blue liner. Shipping Case UPC Code 6477547374. Product of (Country or Countries) is stamped on the case at the time of production.

A label example stated product of USA/China. Photo of case label provided.

Reason

Italian Vegetable Blend product is recalled due to potential to be contaminated with Listeria monocytogenes.

Products involved

Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.

  • Italian Vegetable Blend. Product is frozen, not ready to eat, label carries cooking instruction. Label reads in part "***GARDEN FRESH***64775***47374***ITALIAN BLEND CONTAINS: ZUCCHINI, CARROTS, CAULIFLOWER, LIMAS, ITALIAN BEANS***20 LB NET WT***" No UPC on blue liner. Shipping Case UPC Code 6477547374. Product of (Country or Countries) is stamped on the case at the time of production.

    A label example stated product of USA/China. Photo of case label provided.

Code information listed by FDA

Lot Code Information Item # - 64775-47374 - 29725-4K08D3N, 30604-5B03K3N. and 30604-5B03L3N with corresponding expiration dates 10/8/2016, 2/3/2017, and 2/3/2017.

Distribution and firm information

Recalling firm listed by FDA: National Frozen Foods Corporation--Seattle

Firm location listed by FDA: Seattle, WA, United States

Distribution reported by FDA: distributed nationwide

Product quantity listed by FDA: 3,217 cases or 64,340 lbs.

Source

Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.

Official FDA openFDA food enforcement record

Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.