Class IICompletedVoluntary: Firm initiated
United States Bakery: food recall H-0949-2026
United States Bakery of Eugene, OR recalled Great Value Hawaiian Roll 4pk, Item # F63384. Product is perishable dinner roll ready to eat, sold in a corrugated… Reason: Firm observed oily and sticky substance on direct food contact surface packaging of finished product. The FDA listed it as Class II in its Enforcement Report dated Jun 24, 2026; distribution: Alabama, Arkansas, Arizona, California, Florida, Georgia, Illinois, Indiana, Louisiana, Maine, Minnesota, Missouri, Mississippi, North Carolina, Nebraska, New Mexico, New York, Ohio, Oklahoma, Pennsylvania, South Carolina, Texas, Utah, Virginia, Wisconsin, Wyoming.
Record status as published: Completed. 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
- Great Value Hawaiian Roll 4pk, Item # F63384. Product is perishable dinner roll ready to eat, sold in a corrugated case of 18 packages (4.5oz net wt.) individually wrapped in laminated film. This product was never sold in stores and was never available for consumer purchase. All affected product remained at wholesale distribution centers and has been accounted for.
- Product quantity
- 10,447 cases
- Reason for recall
- Firm observed oily and sticky substance on direct food contact surface packaging of finished product.
- Codes, lots and dates on the package
- W1 116 Julian Codes: 116 119 120 127 134 135 Dates of Production: 4/26/2026 4/29/2026 4/30/2026 5/7/2026 5/14/2026 5/15/2026
- Distribution pattern
- Distributed in AL, AR, AZ, CA, FL, GA, IL, IN, LA, ME, MN, MO, MS, NC, NE, NM, NY, OH, OK, PA, SC, TX, UT, VA, WI, and WY.
- Recalling firm
- United States Bakery, Eugene, OR
- 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 | May 15, 2026 |
| Classified by the FDA | Jun 16, 2026 |
| Published in the Enforcement Report | Jun 24, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0949-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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