Class IITerminatedVoluntary: Firm initiated
JJ Nuts, LLC: food recall F-0733-2025
JJ Nuts, LLC of Fairfield, NJ recalled MAGIC FLAME, HULLED SUNFLOWER KERNELS, BAKERY GRADE, 501b. Bag, Three ply Paper bags, 1100 Paper bags x 50 Ib. on 20… Reason: Glass fragments found in finished product. The FDA listed it as Class II in its Enforcement Report dated Apr 30, 2025; distribution: Maryland, Pennsylvania.
Record status as published: Terminated (terminated Jul 8, 2025). 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
- MAGIC FLAME, HULLED SUNFLOWER KERNELS, BAKERY GRADE, 501b. Bag, Three ply Paper bags, 1100 Paper bags x 50 Ib. on 20 pallets. Store in dry warehouse, room temperature
- Product quantity
- 560 Bags
- Reason for recall
- Glass fragments found in finished product.
- Codes, lots and dates on the package
- Lot#POl544 Pull Date: 12/28/2024 Code #: SUNBGB-50
- Distribution pattern
- The recalled product was distributed to MD, PA
- Recalling firm
- JJ Nuts, LLC, Fairfield, 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
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Apr 13, 2025 |
| Classified by the FDA | Apr 22, 2025 |
| Published in the Enforcement Report | Apr 30, 2025 |
| Terminated | Jul 8, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0733-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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