Ziegenfelder Budget $aver Monster Cherry-Pineapple Pops Recall: Listeria Risk
Ziegenfelder recalls Budget $aver Monster Cherry-Pineapple Pops due to Listeria monocytogenes found in Denver plant samples. Consumers should check lot codes D09418A-D10018B for affected products.
Lower-risk 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.
Contact the company
What happened, in plain English
Ziegenfelder is recalling Budget $aver Monster Cherry-Pine: Pineapple Pops because Listeria bacteria were found in their Denver plant. This could cause serious illness if eaten. Read more at govinfonow.com/recall/19195-ziegenfelder-budget-aver-monster-cherry-pineapple-pops-recall-listeria-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/19195-ziegenfelder-budget-aver-monster-cherry-pineapple-pops-recall-listeria-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-1399-2018
Cite this page
“Ziegenfelder Budget $aver Monster Cherry-Pineapple Pops Recall: Listeria Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19195-ziegenfelder-budget-aver-monster-cherry-pineapple-pops-recall-listeria-risk. Based on FDA recall #F-1399-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1399-2018%22&limit=1).
Why it’s dangerous
Listeria monocytogenes bacteria can cause serious infections, especially in pregnant women, newborns, and the elderly. The bacteria was found in environmental samples at Ziegenfelder's Denver plant during a health inspection.
Who’s affected
People who bought Budget $aver Monster Cherry-Pineapple Pops with lot codes D09418A through D10018B from stores in the U.S. are affected. Pregnant women and young children are at higher risk for serious illness from Listeria.
How to tell if you have this one
Check the lot code on the product label, which ranges from D09418A to D10018B. The product is labeled as Budget $aver Monster Cherry-Pineapple Pops with a net content of 36 fluid ounces.
- Brand
Ziegenfelder- Category
Food
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- 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.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-1398-2018 | Budget $aver Sugar Free Twin Pops Net Contents 28.2 FL OZ; Lot codes D09318A through D10018B | 1,176 cases |
| F-1399-2018 | Budget $aver Monster Cherry-Pineapple Pops Net Contents 36 FL OZ; Lot codes D09418A through D10018B | 2,340 cases |
What to do — step by step
Check Product Lot Code
Look for the lot code on the product label, which should be between D09418A and D10018B.
Where it went and when
Where it was distributed
Distributed in 15 states.
FDA 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.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Arkansas, Florida, Maine, Missouri, Nebraska, Nevada, New Mexico, New York, Ohio, Oklahoma, Texas, Utah, Washington, Wyoming.
Recall timeline
FDA terminated this recall 15 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-1399-2018 (April 23, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1399-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.