FDA recall record
Aminature L-Cysteine HCl Anhydrous 100 mesh 25KG DRUM
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 September 3, 2020. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Aminature L-Cysteine HCl Anhydrous 100 mesh 25KG DRUM
Reason
Foreign material, metal
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.
Aminature L-Cysteine HCl Anhydrous 100 mesh 25KG DRUM
Code information listed by FDA
Lot Numbers: IABF181011; IABF190802; IABF190926
Distribution and firm information
Recalling firm listed by FDA: Cj Haide (Ningbo) Biotech Co., Ltd
Firm location listed by FDA: Ningbo, N/A, China
Distribution reported by FDA: NJ, CT, CA, FL
Product quantity listed by FDA: 193 drums
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.