FDA recall record

Grain Processing Pure Dent B700 Food Corn Starch packaged in 50 lb bags recall — FDA F-0794-2020

A customer reported the presences of metal slivers ranging in length between 1 mm and 30 mm in corn starch ingredient.

Class IIclassification
F-0794-2020official record ID
Mar 11, 2020report date

Recall record at a glance

Official recordF-0794-2020
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmGrain Processing Corporation
Report dateMar 11, 2020
Recall initiation dateFeb 20, 2020
Quantity3790 bags
LocationMuscatine, IA, United States

Official product description

Pure Dent B700 Food Corn Starch packaged in 50 lb bags

Why the product was recalled

A customer reported the presences of metal slivers ranging in length between 1 mm and 30 mm in corn starch ingredient.

Distribution information

Distributed to customers in KY, OH, MN, MO, WI and internationally to Canada.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.