STAR WARS TIN WITH CARAMEL POPCORN NET WT 3.5 oz (99g) CONTAINS MILK AND SOY, MAY…
Ross Acquisitions Company recalled this product and the FDA reported the enforcement action on 21 February 2018 as Class II. The recall was initiated by the firm. The firm was notified by a customer that the popcorn in the product contains grain beetles.

The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- STAR WARS TIN WITH CARAMEL POPCORN NET WT 3.5 oz (99g) CONTAINS MILK AND SOY, MAY CONTAIN TREE NUTS AND PEANUTS DISTRIBUTED BY GALERIE HEBRON, KENTUCKY 41048 UPC 7 68395 51585 0
- UPC
- 768395515850
- Reason for recall
- The firm was notified by a customer that the popcorn in the product contains grain beetles.
- Recalling firm
- Ross Acquisitions Company
- Firm location
- Hebron, Kentucky, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-0821-2018
- Quantity
- 9,800 units
- Distribution
- Product was shipped to the following states: AL, AZ, CA, CO, GA, IA, IN, KS, KY, MI, MN, NC, NY, OH, OR, PA, SC, TX, VA & WI.
- Initiated
- 2 February 2018
- Reported by FDA
- 21 February 2018
- Terminated
- 4 April 2018
- Firm notified by
- Letter
- Product codes
- BESTBY 30SEPT2018 Packing Lot Code 76579 324 A3 HB, Product Lot Code (Tin) 30830 3455-0349/50 244, Food Lot Code (On Bag of Popcorn) A7262
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This record is the only one the FDA opened for its recall event, so it covers a single product code.
- The recall ran for 2 months, from 2 February 2018 to termination on 4 April 2018. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 17 states, and the FDA published the enforcement report 3 weeks after the firm began the recall.
- Recalls of milk or a dairy product run a median of 7 months, so this one was shorter than usual for its category. Dairy recalls split between pathogen contamination in products that skipped or under-ran pasteurisation and undeclared milk in products that should never have contained it, which is the same allergen viewed from two directions.
Named in the distribution pattern: Arizona, California, Colorado, Georgia, Iowa, Indiana, Kansas, Kentucky, Michigan, Minnesota, North Carolina, New York, Ohio, Oregon, Pennsylvania, South Carolina, Texas. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
Filed under milk and dairy, nuts and seeds and snacks and confectionery. A product can sit in more than one.
Other milk and dairy recalls
These are the closest records in the corpus: the same kind of food. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
All 2018 recalls · All FDA food recall data
Behind every recall is a clause somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.