'KORICA' ROASTED PEANUT; 10.6OZ (300G); packaged in plastic bags; Ingredients: Peanuts…
Rong Shing Trading NY Inc recalled this product and the FDA reported the enforcement action on 18 May 2022 as Class III. The recall was initiated by the firm. Product contains cyclamate, an unapproved 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
- 'KORICA' ROASTED PEANUT; 10.6OZ (300G); packaged in plastic bags; Ingredients: Peanuts, Salt, Licorice, Anise, Cinnamon, Food Additives (Cyclamate); Product of P.R.C.; Manufacturer: Jianmen Xinhui Green Day Food Co. Ltd.; RONG SHING TRADING NY INC. 47-57 BRIDGEWATER STREET BROOKLYN NY 11222
- Reason for recall
- Product contains cyclamate, an unapproved color.
- Recalling firm
- Rong Shing Trading NY Inc
- Firm location
- Brooklyn, New York, United States
- Classification
- Class III
- Status
- Terminated
- Recall number
- F-1059-2022
- Quantity
- N/A
- Distribution
- IL, IN, WA, NY, NJ, FL, MN, CT, MA, CA, PA & WI
- Initiated
- 18 April 2022
- Reported by FDA
- 18 May 2022
- Terminated
- 26 August 2022
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- UPC_6950296804537 & Best Before 06/15/2023
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class III means the FDA judged that the product was unlikely to cause harm but violated FDA labelling or manufacturing regulation. 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 4 months, from 18 April 2022 to termination on 26 August 2022. 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 10 states, and the FDA published the enforcement report 4 weeks after the firm began the recall.
- Recalls of nuts or seeds run a median of 7 months, so this one was shorter than usual for its category. Nuts and seeds carry both hazards at once: they are a major allergen in their own right, and as a low-moisture food they hold Salmonella for months without supporting its growth, which is why a nut butter recall can trace to a lot pressed a year earlier.
Named in the distribution pattern: Illinois, Indiana, Washington, New York, New Jersey, Florida, Minnesota, Connecticut, Massachusetts, California. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
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 nuts and seeds and spices and seasonings. A product can sit in more than one.
Other nuts and seeds 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 Rong Shing Trading NY Inc
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 10 other records name this firm.
All 11 records for Rong Shing Trading NY Inc
All 2022 recalls · All FDA food recall data
21 CFR 111 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.