MEI HEONG YUEN GARLIC FLAVOR ROASTED PEANUTS; 9.17 oz (260g); Ingredients: Peanuts…
Super World Trading Inc. recalled this product and the FDA reported the enforcement action on 8 April 2026 as Class III. The recall was initiated by the firm. Products contain cyclamates (banned sweetener)
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
- MEI HEONG YUEN GARLIC FLAVOR ROASTED PEANUTS; 9.17 oz (260g); Ingredients: Peanuts, Salt, Garlic, Liquorice, Sugar, Saccharin; Shelf Life: 18 Months; Manufacturer: Heshan Mei Heong Yuen Food Pte Ltd; Distributor in USA: Super World Trading Inc 28 Varick Ave. Brooklyn, NY 11237; UPC: 6912449124329
- UPC
- 6912449124329
- Reason for recall
- Products contain cyclamates (banned sweetener)
- Recalling firm
- Super World Trading Inc.
- Firm location
- Brooklyn, New York, United States
- Classification
- Class III
- Status
- Terminated
- Recall number
- H-0643-2026
- Quantity
- 595 cases (total)
- Distribution
- CO, CT, DE, FL, GA, IL, MA, MD, MI, NY, NC, NJ, OH, OR, PA, TX, UT, VA, WA
- Initiated
- 19 February 2026
- Reported by FDA
- 8 April 2026
- Terminated
- 21 July 2026
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- MFD: 20250710, EXP:20270109, FIRM CODE: 401021
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 is one of 3 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 3 separate recalls, which almost every published figure does, overstates it by a factor of 3. 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 3 of them.
- The recall ran for 5 months, from 19 February 2026 to termination on 21 July 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 19 states, and the FDA published the enforcement report 7 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: Colorado, Connecticut, Delaware, Florida, Georgia, Illinois, Massachusetts, Maryland, Michigan, New York, North Carolina, New Jersey, Ohio, Oregon, Pennsylvania, Texas, Utah, Virginia, Washington. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
Filed under nuts and seeds and spices and seasonings. A product can sit in more than one.
Other nuts and seeds recalls
These are the closest records in the corpus: the same kind of food. 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 Super World Trading Inc.
The FDA opens one enforcement record per product code, so several of these are frequently one recall event.
All 4 records for Super World Trading Inc.
All 2026 recalls · All FDA food recall data
Behind every recall is a clause 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.