Ocinet, Inc., of Downey, California, is recalling all “…And Kimchi” branded sliced kimchi, UPC 8541200408, UPC 8541200409, and UPC 8541200411 (the “Product”) because the Product contains undeclared fish (anchovies). People who have an allergy or severe sensitivity to fish run the risk of a serious or life-threatening allergic reaction if they consume this Product.
The recalled Product was distributed to six retail locations:
- Zion Market – 8330 Clairemont Mesa Blvd., San Diego, CA 92111
- Zion Market – 4800 Irvine Blvd, Irvine, CA 92620
- Zion Market – 750 S Oxford Ave, Los Angeles, CA 90005
- Zion Market – 5400 Beach Blvd., Buena Park, CA 90621
- Zion Market – 2340 Pleasant Hill Rd., Duluth, GA 30096
- Zion Market – 2405 S Stemmons Fwy, Lewisville, TX 75067
The Product is sold in a 126 oz (3.57 kilogram) clear plastic jar, a 63 oz (1.78 kilogram) clear plastic jar, and a 30 oz (850 gram) clear plastic jar, all marked with the “… And Kimchi” logo in red font. The UPC numbers are 8541200408 (126 oz jar), 8651200409 (63 oz jar), and 8541200411 (30 oz jar). Product images for the 126 oz jar are below.
No illnesses have been reported to date.
The recall was initiated after it was discovered that the Product was distributed in packaging that did not reveal the presence of fish. Distribution of the Product has been suspended until the company is certain that the problem has been corrected.
Consumers who have purchased this Product and have concerns about the inclusion of the allergen are welcome to return the Product to the retail store where any such Product was purchased for a full refund.
Consumers with questions may contact the retail store where the product was purchased as set forth below:
- Zion Market – San Diego, CA, (858) 268-3300
- Zion Market – Irvine, CA, (714) 832-5600
- Zion Market – Los Angeles, CA, (213) 302-3792
- Zion Market – Buena Park, CA, (714) 367-5400
- Zion Market – Duluth, GA, (770) 813-3200
- Zion Market – Lewisville, TX, (972) 315-1734
The retail stores may also be contacted via email with any questions at [email protected].
Or, consumers may contact the manufacturer at:
Ocinet, Inc.
Recall Manager
[email protected]
Second Nature Brands of Madison Heights, MI, is voluntarily recalling certain 10-ounce packages of SECOND NATURE KETO CRUNCH SMART MIXTM because the product may contain undeclared cashews, pistachios, and cherries.
Individuals who have an allergy or severe sensitivity to tree nuts, including cashews and pistachios, or to cherries, may be at risk of serious or life-threatening allergic reactions if they consume this product.
The affected product was distributed nationwide in retail stores and through online orders.
The product comes in a 10-ounce pouch with UPC 077034013405. Affected pouches are marked with “Best if used by 2/12/2027” on the backside of pouch. Packages with other Best if used by dates are not affected.
No illnesses have been reported to date in connection with this issue.
The recall was initiated after it was discovered that product containing cashews, pistachios, and cherries was distributed in packaging that did not reveal the presence of these allergens. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company’s production and packaging processes. Consumers who have purchased 10-ounce packages of Second Nature Keto Crunch Smart Mix with Best if used by 2/12/2027 should not consume the product and should contact Second Nature Brands for a full refund.
Consumers may contact the company by calling +1.800.651.7263 Monday-Friday from 8:00AM to 8:00PM ET, Saturday-Sunday from 9:00AM to 5:00PM ET or via [email protected].
Second Nature Brands is committed to the safety and quality of its products and is taking immediate steps to correct the issue and prevent recurrence.
Second Nature Brands is conducting this recall with the knowledge of the U.S. Food and Drug Administration.
The a2 Milk Company (“a2MC”) has voluntarily recalled three specific batches of its imported a2 Platinum Premium USA label infant formula 0-12 months (“Product”) due to the presence of cereulide. The Product is sold only in the United States.
Cereulide is a heat-stable toxin produced by some strains of the bacterium Bacillus cereus. Illness occurs through the consumption of food contaminated with the toxin and preparing formula with hot water does not eliminate it.
Symptoms typically develop within 30 minutes to six hours of ingestion and most often involve gastrointestinal symptoms such as nausea and vomiting that typically self-resolve within 24 hours. Infants are at greater risk due to their developing immune systems and can experience complications such as dehydration which require medical care.
Product Information
Product Name
Packaging Format
Batch Number
Use By Date
a2 Platinum Premium infant formula 0-12 months Milk-based powder with Iron
31.7oz tin
2210269454
7/15/2026
31.7oz tin
2210324609
1/21/2027
31.7oz tin
2210321712
1/15/2027
The batch number and “Use By” (expiration) date are found on the bottom of each tin (refer to example below).
The Product was distributed nationally through a2MC’s website, Amazon and Meijer stores as part of Operation Fly Formula. Importation rights expired on December 31st, 2025, and the Product has been discontinued and removed from sale prior to the initiation of the recall. The total number of units in the three batches is 63,078 of which an estimated 16,428 units were sold to consumers.
Although no confirmed incidents of illness or harm have been reported, affected batches must not be used.
The recall was initiated by a2MC after cereulide was detected through additional testing of the Product conducted in response to new guidance issued by New Zealand’s food regulatory authority. The probable source of cereulide is an ingredient in the Product.
This recall is being made with the knowledge of the U.S. Food and Drug Administration.
Consumers who have purchased the Product are recommended to discontinue use of the Product and dispose of it immediately or return to their place of purchase for a refund. If your infant is experiencing symptoms described above, contact your health care provider immediately. To report an illness or adverse event to the FDA, you can:
- Report a Product Problem through SmartHub, or
- Complete and submit a Medwatch report Online at www.fda.gov/medwatch/report.htm, or by Regular Mail or Fax: Download the form from www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
Consumers with questions may contact a2MC at 1-844-422-6455, Monday-Friday, 8am to 5pm Eastern time zone, or contact us through our website on a2platinum.com.
