FDA recall record
TK006 Van Krimpet Powder Blend 50#. Item number 4107780
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 August 28, 2023. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
TK006 Van Krimpet Powder Blend 50#. Item number 4107780
Reason
Product may be contaminated with 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.
TK006 Van Krimpet Powder Blend 50#. Item number 4107780
Code information listed by FDA
Batch Numbers 0010636568 and 1110644921,
Distribution and firm information
Recalling firm listed by FDA: Puratos Corporation (HQ and Innovation Center)
Firm location listed by FDA: Pennsauken, NJ, United States
Distribution reported by FDA: Distributed to domestic customers in CA, NJ, IN, PA, TN, NY, NC, TX, FL, DE, LA, and LA. Distributed to foreign customers in Dominican Republic and Trinidad.
Product quantity listed by FDA: 30,350 lbs
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.