1) Simply Orange Pulp Free Orange Juice, 46 FL OZ (1.4 QT) 1.36 L, packaged in a plastic…
Dollar General Corporation recalled this product and the FDA reported the enforcement action on 13 August 2025 as Class II. The recall was initiated by the firm. Temperature abuse due to temperature excursion in one shipping trailer
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
- 1) Simply Orange Pulp Free Orange Juice, 46 FL OZ (1.4 QT) 1.36 L, packaged in a plastic bottle, UPC: 025000136788 2) Simply Orange Pulp Free Orange Juice, 11.5 FL OZ (340 mL), packaged in a plastic bottle, UPC: 025000000249
- UPC
- 0250001367882
- Reason for recall
- Temperature abuse due to temperature excursion in one shipping trailer
- Recalling firm
- Dollar General Corporation
- Firm location
- Goodlettsville, Tennessee, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- H-0414-2025
- Quantity
- 1) 1 eaches; 2) 1 eaches; 2 eaches TOTAL
- Distribution
- LA
- Initiated
- 14 July 2025
- Reported by FDA
- 13 August 2025
- Terminated
- 6 March 2026
- Firm notified by
- Telephone
- Product codes
- Exact lot codes/expiration dates are unknown.
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 is one of 24 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 24 separate recalls, which almost every published figure does, overstates it by a factor of 24. All 24 of them are listed on this page.
- The recall ran for 8 months, from 14 July 2025 to termination on 6 March 2026. 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 1 state, and the FDA published the enforcement report 4 weeks after the firm began the recall.
- Recalls of a beverage or juice run a median of 6 months, so this one was about typical for its category. Juice is the other food with its own HACCP regulation in the United States, 21 CFR part 120, which requires a treatment achieving a 5-log reduction of the pertinent pathogen, and unpasteurised juice recalls are almost always a failure of that step or an exemption misapplied.
What this recall was for
Process deviation
A process deviation recall means the process ran outside its validated limits: a thermal process that did not reach its time and temperature, a pH that drifted, or a seal that failed.
A preventive controls plan covers a process deviation under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 113
- Thermally processed low-acid foods in hermetically sealed containers: the scheduled process, its establishment by a competent authority, and the records proving every container received it.
- 21 CFR 114
- Acidified foods: the controls on equilibrium pH at or below 4.6, and the process that achieves it.
- 21 CFR 117.150
- Corrective actions: what a facility does when a preventive control was not properly implemented, including identifying and correcting the problem and evaluating the food for safety.
Filed under beverages and juice. A product can sit in more than one.
Every product in this recall
The FDA opened 24 enforcement records for this one recall, one per product code. This page carries all of them; the 23 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.
Other beverages and juice recalls for the same reason
These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2026-05-27 | Pure Libido Drink 16 oz and 32 oz. | LIQUID BLENZ CORP | May be under-processed resulting in growth of Clostridium botulinum and lists health claims. | Class II |
| 2026-02-11 | JUICE from the Raw, cashew milk | Everpress Juice | Under-processed product may contain pathogenic bacteria that could harm to humans. | Class I |
| 2026-02-11 | JUICE from the Raw, cashew coffee milk | Everpress Juice | Under-processed product may contain pathogenic bacteria that could harm to humans. | Class I |
| 2026-02-11 | JUICE from the Raw, pineapple mint | Everpress Juice | Under-processed product may contain pathogenic bacteria that could harm to humans. | Class I |
| 2026-02-11 | JUICE from the Raw, spicy lemonade | Everpress Juice | Under-processed product may contain pathogenic bacteria that could harm to humans. | Class I |
| 2026-02-11 | JUICE from the Raw, upbeat | Everpress Juice | Under-processed product may contain pathogenic bacteria that could harm to humans. | Class I |
| 2026-02-11 | JUICE from the Raw, sweet greens | Everpress Juice | Under-processed product may contain pathogenic bacteria that could harm to humans. | Class I |
| 2026-02-11 | JUICE from the Raw, DETOX GREENS | Everpress Juice | Under-processed product may contain pathogenic bacteria that could harm to humans. | Class I |
Other records from Dollar General Corporation
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 27 other records name this firm.
All 28 records for Dollar General Corporation
All 2025 recalls · All FDA food recall data
21 CFR 113 is the clause behind this recall, and it is one 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.