US Food Recall Atlas

A single recall record, as the agency published it.

Recall map → All recalls → F-1398-2018

Budget $aver Sugar Free Twin Pops Net Contents 28.2 FL OZ Ziegenfelder Company, Inc. · reported 2018-05-16

Terminated This recall has been closed out by the agency.

Reason for recall
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.
Classification
Class II
Recall initiated
2018-04-23
Reported by the agency
2018-05-16
Closed out (terminated)
2019-07-25
Recalling firm
Ziegenfelder Company, Inc.
Wheeling, WV
United States

This is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.

Distribution (the agency's own words)
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.
States we parsed from that text
AL AR FL ME MO NE NM NV NY OH OK TX UT WA WY

The agency named these states. Parse method explicit_state_list, confidence high.

Food category
uncategorised

Assigned by a reviewed keyword rulebook over the product description, not by the agency.

Recall type
Voluntary: Firm initiated
Recall number
F-1398-2018

Verifying this record. Everything above is FDA's own record, reproduced. FDA publishes no web page for an individual enforcement report, so the only direct link is the machine-readable one:

Open the raw FDA record (JSON) →

To look it up yourself, search recall number F-1398-2018 in FDA's Enforcement Report. That search cannot be linked to directly, so the number has to be pasted in.

This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.