refrigerated BEVERAGE 1. PURE GREEN TFM SOUL KICK 16 OZ UPC 1996266053 2.
United Natural Foods, Inc. recalled this product and the FDA reported the enforcement action on 10 August 2022 as Class II. The recall was initiated by the firm. Two food trailers holding various types and brands of frozen foods were temperature abused during deliver to two retail stores.
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
refrigerated BEVERAGE 1. PURE GREEN TFM SOUL KICK 16 OZ UPC 1996266053 2. PURE GREEN TFM WAKE UP CALL 16 OZ UPC 1996266073 3. PURE GREEN TFM GOLDEN GIRL 16 OZ UPC 65334133484 4. COOLBREW COOL BREW MOCHA CFE CNCNTRTE UPC 5372101605 6 16.9FZ NEW ORLEANS COFFEE Co. 5. GT'S GT'S SYNERGY ORGANIC TRILOGY 16FL OZ UPC 72243011000 GTS LIVING FOODS LLC 6. EVOLUTION EVOLUTION GREEN DEVOTION JUICE 11FL. OZ UPC 76235764411 EVOLUTION FRESH INC 7. GT'S SYNERGY ORGANIC & RAW GUAVA GOODNESS KOMBUCHA 16FL OZ UPC 72243090000 12 GTS LIVING FOODS LLC 8. GT'S SYNERGY ORGANIC & RAW GUAVA GOODNESS KOMBUCHA 16FL OZ UPC 72243090000 GTS LIVING FOODS LLC 9. KEVITA KEVITA ORGANIC LEMON CAYENNE JUICE 15.2FL OZ UPC 85331100373 QUAKER SALES & DISTR 10. EVOLUTION EVOLUTION GREEN GROVE JUICE 11FL OZ UPC 76235764211 EVOLUTION FRESH INC 11. GT'S GT'S ORGANIC PINK LADY BASIL KOMBUCHA TEA 16OZ 7640103 72243036000 12 16FZ GTS LIVING FOODS LLC 12. INDIAN RIVER INDIAN RIVER ORANGE JUICE 52FL. OZ UPC 71279710652 INDIAN RIVER SELECT 13. INDIAN RIVER INDIAN RIVER GLUTEN FREE OJ NO PULP 52FL OZ UPC 71279731652 INDIAN RIVER SELECT 14. INDIAN RIVER INDIAN RIVER GLUTEN FREE OJ NO PULP 52FL OZ UPC 71279731652 INDIAN RIVER SELECT 15. INDIAN RIVER INDIAN RIVER ORANGE JUICE+CALCIUM&VIT D 52FL OZ UPC 71279715652 INDIAN RIVER SELECT 16. INDIAN RIVER INDN RIVR RUBY RED GRAPEFRUIT JUICE 52FZ 7643422 71279720652 6 52 FZ INDIAN RIVER SELECT 17. HOIST HOIST SUPER HYDRATION STRAWBERRY LEMONADE HF BTL 16 FL OZ UPC 85952000238 QCK LLC 18. SOFRESCO SO FRESCO COLD PRESSED JUICE LEMON MINT APPLE 12OZ UPC 85000586604 GOOD CROP INC 19. SOFRESCO SO FRESCO COLD PRESSED JUICE CELERY CUKE APPLE 12OZ UPC 85000586602 GOOD CROP INC 20. SOFRESCO SO FRESCO COLD PRESSED JUICE BEET APPLE 12OZ UPC 85000586600 GOOD CROP INC 21. SUJA SUJA ORGANIC CELERY JUICE 12 OZ UPC 81861702261 SUJA LIFE LLC 22. SUJA SUJA ESSENTIALS TURMERIC LOVE 12OZ UPC 81861702186 SUJA LIFE LLC 23. INDNRVR INDIAN RIVER 100% VALENCIA OJ UPC 71279751973 INDIAN RIVER SELECT 24. VITACOCO VITA COCO COCONUT WATER 4PK 67.6FLZ UPC 89899901300 ALL MARKET INC
UPC
1996266053
Reason for recall
Two food trailers holding various types and brands of frozen foods were temperature abused during deliver to two retail stores.
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 15 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 15 separate recalls, which almost every published figure does, overstates it by a factor of 15. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 15 of them.
The recall ran for 13 months, from 16 June 2022 to termination on 27 July 2023. 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 2 states, and the FDA published the enforcement report 8 weeks after the firm began the recall.
Recalls of fresh produce run a median of 7 months, so this one was longer than usual for its category. Fresh produce is the category where contamination arrives before the facility does: irrigation water, soil amendments and field workers are the routes, and nothing downstream of the farm is a kill step for a product eaten raw.
Named in the distribution pattern: Alabama, Mississippi. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
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.
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.
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.
Recall 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.
