Skip to main content
High RiskFDAfda-F-1399-2018LISTERIA

Budget $aver Monster Cherry-Pineapple Pops Net Contents 36 FL OZ

Category
Units Affected
2,340
Recall Date
April 23, 2018
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1399-2018.

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.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1399-2018.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Ziegenfelder Company, Inc. or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1399-2018.

Ziegenfelder Company, Inc.

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

Visit FDA.gov →

📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

How to report to FDAFile a report at FDA

Ziegenfelder Company, Inc. Recall FAQ

Ziegenfelder Company, Inc. is the subject of a food safety report: Budget $aver Monster Cherry-Pineapple Pops Net Contents 36 FL OZ. The notice was published on April 23, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 2,340 units are potentially affected.