Class IITerminatedVoluntary: Firm initiated
TROPICANA BRANDS GROUP: food recall H-0073-2026
TROPICANA BRANDS GROUP of Chicago, IL recalled Dole Apple Juice (primary package), 15.2 Fl oz., PET, 12 bottles per case, Refrigerate after opening. Reason: A manufacturing process deviation occurred which may cause spoilage or microbial contamination and affect shelf stability. The FDA listed it as Class II in its Enforcement Report dated Oct 22, 2025; distribution: Arkansas, Colorado, Iowa, Kansas, Missouri, Mississippi, Nebraska, New Mexico, Oklahoma, Tennessee, Texas.
Record status as published: Terminated (terminated Apr 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
- Dole Apple Juice (primary package), 15.2 Fl oz., PET, 12 bottles per case, Refrigerate after opening
- Product quantity
- 1,599 cases
- Reason for recall
- A manufacturing process deviation occurred which may cause spoilage or microbial contamination and affect shelf stability.
- Codes, lots and dates on the package
- Case Code: Jan 10 26 xxxx(military time) ET 1 Primary Package code: (first line) Jan 10 26 CT127 (second line) XXXX (military time) ET071452
- Distribution pattern
- The adulterated product was distributed to the following states: AR, CO, IA, KS, NE, MO, TX, MS, TN, NM, OK,
- Recalling firm
- TROPICANA BRANDS GROUP, Chicago, IL
- 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
- Telephone
Advertisement
Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Sep 11, 2025 |
| Classified by the FDA | Oct 16, 2025 |
| Published in the Enforcement Report | Oct 22, 2025 |
| Terminated | Apr 6, 2026 |
Advertisement
OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.
Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0073-2026 (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.