Sunbest Natural Lemon Juice 33.5 Fl. Oz. Distributed by Sunco & Frenchie LLC Clifton, NJ…
SUNCO & FRENCHIE LLC. recalled this product and the FDA reported the enforcement action on 17 February 2016 as Class II. The recall was initiated by the firm. Lemon juice contains unapproved color and undeclared color.
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
- Sunbest Natural Lemon Juice 33.5 Fl. Oz. Distributed by Sunco & Frenchie LLC Clifton, NJ 07011 UPC 089625403007
- UPC
- 089625403007
- Reason for recall
- Lemon juice contains unapproved color and undeclared color.
- Recalling firm
- SUNCO & FRENCHIE LLC.
- Firm location
- Clifton, New Jersey, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-0578-2016
- Quantity
- 1736 cases (12 bottles per case)
- Distribution
- NY
- Initiated
- 4 December 2015
- Reported by FDA
- 17 February 2016
- Terminated
- 23 June 2017
- Firm notified by
- Letter
- Product codes
- LOT: IHR1
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 19 months, from 4 December 2015 to termination on 23 June 2017. 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 2 months after the firm began the recall.
- Recalls of a beverage or juice run a median of 6 months, so this one was longer than usual 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
Undeclared allergens
An undeclared allergen recall means a food contained one of the major allergens and the label did not say so, either because the wrong label was applied or because an ingredient carried an allergen nobody traced.
A preventive controls plan covers an undeclared allergen 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 117.135(c)(2)
- Food allergen controls: the written preventive controls that keep an allergen out of a food it does not belong in, and that get the allergens present onto the label.
- 21 CFR 101.4
- Ingredient declaration: every ingredient listed by its common name, in descending order of predominance, on the label of a packaged food.
- 21 CFR 117 subpart G
- Supply-chain programme: the approval and verification a receiving facility runs on a supplier when the hazard is controlled before the ingredient arrives.
Unapproved ingredients
An unapproved ingredient recall means a product contained a substance not permitted in food, most often an undisclosed pharmaceutical active found in a dietary supplement.
A preventive controls plan covers an unapproved ingredient 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 111
- Dietary supplement CGMP: the identity, purity, strength and composition specifications a supplement manufacturer sets and verifies for every component and finished batch.
- 21 CFR 117 subpart G
- Supply-chain programme: the approval and verification a receiving facility runs on a supplier when the hazard is controlled before the ingredient arrives.
Filed under beverages and juice. A product can sit in more than one.
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.
Other records from SUNCO & FRENCHIE LLC.
The FDA opens one enforcement record per product code, so several of these are frequently one recall event.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2024-09-11 | Terrafina Golden Raisins Net Wt. 10oz (283g) UPC:847938001385. Packaged in a plastic container, 8 containers per case. | SUNCO & FRENCHIE LLC. | Undeclared sulfites | Class I |
| 2024-07-24 | Terrafina, Macadamia in the Raw , Net Wt. 6oz , (170 g) | SUNCO & FRENCHIE LLC. | Product tested positive for presence of salmonella. | Class I |
All 3 records for SUNCO & FRENCHIE LLC.
All 2016 recalls · All FDA food recall data
21 CFR 117.135(c)(2) 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.