Class IIOngoingVoluntary: Firm initiated
Dr. Praeger's Sensible Foods Inc.: food recall F-0694-2025
Dr. Praeger's Sensible Foods Inc. of Elmwood Park, NJ recalled Dr. Praeger s California Veggie Fries 8oz,. Reason: Undeclared Allergen (Soy). The FDA listed it as Class II in its Enforcement Report dated Apr 16, 2025; distribution: California, Colorado, Connecticut, Florida, Georgia, Illinois, Indiana, Massachusetts, Maryland, New Hampshire, New Jersey, New York, Pennsylvania, Texas, Wisconsin.
Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Dr. Praeger s California Veggie Fries 8oz,
- Product quantity
- 8,665 cases.
- Reason for recall
- Undeclared Allergen (Soy)
- Codes, lots and dates on the package
- UPC 80868-1931404, LOT NUMBER I24BI-01A
- Distribution pattern
- The adulterated product was distributed to the following states: CT, MA, IL, MD, NY, PA, TX, CA, IN, CO, NH, WI, GA, NJ, FL
- Recalling firm
- Dr. Praeger's Sensible Foods Inc., Elmwood Park, NJ
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Telephone
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Apr 1, 2025 |
| Classified by the FDA | Apr 7, 2025 |
| Published in the Enforcement Report | Apr 16, 2025 |
Other recalls by Dr. Praeger's Sensible Foods Inc.
- H-0570-2026 · Mar 25, 2026 · Class II — This product has the possibility of contamination with rodent hair.
- H-0151-2026 · Nov 12, 2025 · Class II — Product was made on equipment that test positive for Listeria .
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0694-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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