Garden Gate Tofu (Golden Gate Soy) – Listeria risk (2019)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Garden Gate Tofu, Firm; Ingredients: Soybean, Filter water, Calcium Sulfate. Contains: soy Sold in 60 piece (bulk box) and 18 piece packages 73 oz. - UPC 7 83301 96198 1 Pasteurized/Perishable. Keep Refrigerated. Made in USA.
Brand
Golden Gate Soy Products, Inc.
Lot Codes / Batch Numbers
18 piece - all expiration dates up to and including 3/27/2019, 60 piece tofu - all expiration dates up to and including 3/6/19.
Products Sold
18 piece - all expiration dates up to and including 3/27/2019; 60 piece tofu - all expiration dates up to and including 3/6/19.
Golden Gate Soy Products, Inc. is recalling Garden Gate Tofu, Firm; Ingredients: Soybean, Filter water, Calcium Sulfate. Contains: soy So due to FDA sampling found Listeria monocytogenes in zone 1 and 2 food contact surfaces.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
FDA sampling found Listeria monocytogenes in zone 1 and 2 food contact surfaces.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA
Page updated: Jan 6, 2026