FDA recall record
MBF-202 Carrageenan
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 April 28, 2021. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
MBF-202 Carrageenan
Reason
On August 28, 2020, the firm's customer discovered colored fibers up to 1/4 " in length after sifting a lot of finished carrageenan intended for use as an ingredient in a finished food product. The fibers were identified by the recalling firm as 'tie tie' a fibrous rope used for seaweed production that was present in the seaweed ingredient used to manufacture carrageenan.
One August 28, 2020 the firm recalled the finished carrageenan.
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.
MBF-202 Carrageenan
Code information listed by FDA
191001-A 191001-B 191002-A Use by dates: 10/01/21 & 10/02/21 191002-B 191003-A
Distribution and firm information
Recalling firm listed by FDA: Ingredients Solutions Inc.
Firm location listed by FDA: Waldo, ME, United States
Distribution reported by FDA: IA, KS, WI, KY
Product quantity listed by FDA: 18,000 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.