Class IITerminatedVoluntary: Firm initiated
Blooming Import Inc.: food recall F-0717-2025
Blooming Import Inc. of Brooklyn, NY recalled Golden Crop Candy (8 oz. (227g) un-wrapped candies). Reason: Contains undeclared and unallowed colors (Blue 1, Red 40, Acid Red 18). The FDA listed it as Class II in its Enforcement Report dated Apr 23, 2025; distribution: Delaware, Massachusetts, Maryland, Missouri, New Jersey, New York, Pennsylvania, Texas.
Record status as published: Terminated (terminated Mar 6, 2026). 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
- Golden Crop Candy (8 oz. (227g) un-wrapped candies)
- Product quantity
- 74 cases total
- Reason for recall
- Contains undeclared and unallowed colors (Blue 1, Red 40, Acid Red 18)
- Codes, lots and dates on the package
- UPC Code: 734765134587
- Distribution pattern
- NY, PA, MD, NJ, MA, MO, DE, TX
- Recalling firm
- Blooming Import Inc., Brooklyn, NY
- 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
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Mar 5, 2025 |
| Classified by the FDA | Apr 16, 2025 |
| Published in the Enforcement Report | Apr 23, 2025 |
| Terminated | Mar 6, 2026 |
Other products in the same recall event
The FDA groups related products under one recall event (event 96505).
- F-0716-2025 — Golden Crop Candy (10 oz. (283g) wrapped candies)
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0717-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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