Food recall: Budget $aver Sugar Free Twin Pops Net Contents 28.2 FL OZ
Ziegenfelder Company, Inc. (Wheeling, WV) initiated this food recall on 23 Apr 2018; FDA lists 2 product records under event 79931, classified Class II.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 56% of the 578 food enforcement events initiated in 2018 carry the same class.
Status: Terminated, terminated 25 Jul 2019. Initiation: voluntary: firm initiated. This is the only enforcement event on this register for Ziegenfelder Company, Inc..
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Ziegenfelder Company, Inc., Wheeling, WV.
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."
Distribution
"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 records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1398-2018 | Budget $aver Sugar Free Twin Pops Net Contents 28.2 FL OZ | 1,176 cases | Class II | Terminated | 16 May 2018 |
| F-1399-2018 | Budget $aver Monster Cherry-Pineapple Pops Net Contents 36 FL OZ | 2,340 cases | Class II | Terminated | 16 May 2018 |
Context
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "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."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "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."
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 25 Jul 2019. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.