FDA recall record
Kabayaki Unagi Bits (Broiled Eel Bits) Tetsujin
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of February 9, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Kabayaki Unagi Bits (Broiled Eel Bits) Tetsujin
Reason
Potential Listeria monocytogenes contamination.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Kabayaki Unagi Bits (Broiled Eel Bits) Tetsujin
Code information listed by FDA
Manufacture date code: 160526 Manufacture date code: 180526 Lot#: 160526013600Y0027032
Distribution and firm information
Recalling firm listed by FDA: Ming Hong International,Inc.
Firm location listed by FDA: City Of Industry, CA, United States
Distribution reported by FDA: U.S. distribution to the following, CA, NM, HI, OR, AZ. No foreign distirbution.
Product quantity listed by FDA: 352 cases
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.