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FDA recall record

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Recall F-1399-2018Class IITerminatedApril 23, 2018

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 July 25, 2019. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

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Reason

The Colorado Department of Public Health & Environment notified the firm that they had recovered Listeria monocytogenes from multiple environmental sampling sites collected during an inspection at their Denver plant.

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.

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Code information listed by FDA

Lot codes D09418A through D10018B

Distribution and firm information

Recalling firm listed by FDA: Ziegenfelder Company, Inc.

Firm location listed by FDA: Wheeling, WV, United States

Distribution reported by FDA: Product distributed to retail stores and distributors in Alabama, Arkansas, Florida, Maine, Missouri, Nebraska, Nevada, New Mexico, New York, Ohio, Oklahoma, Texas, Utah, Washington and Wyoming.

Product quantity listed by FDA: 2,340 cases

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.