Class IITerminatedVoluntary: Firm initiated
BlueStar Direct LLC: food recall F-0069-2025
BlueStar Direct LLC of Warren, NJ recalled Dry Dates, 50 lb. bag. Reason: No label- Undeclared sulfur dioxide. The FDA listed it as Class II in its Enforcement Report dated Oct 30, 2024; distribution: Illinois.
Record status as published: Terminated (terminated Feb 7, 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
- Dry Dates, 50 lb. bag
- Product quantity
- 40 Bags
- Reason for recall
- No label- Undeclared sulfur dioxide
- Codes, lots and dates on the package
- Unknown
- Distribution pattern
- The recall product was distributed to one Consignee, Chetak Chicago LLC 1111 Lake St, Streamwood, IL 60107 .
- Recalling firm
- BlueStar Direct LLC, Warren, 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
- Letter
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Aug 26, 2024 |
| Classified by the FDA | Oct 24, 2024 |
| Published in the Enforcement Report | Oct 30, 2024 |
| Terminated | Feb 7, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0069-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.