FDA recall record

Ingredion Fermentation Derived Pepsin Product packaging: 5 individual recall — FDA F-0956-2021

Undeclared egg allergen

Class IIclassification
F-0956-2021official record ID
Sep 15, 2021report date

Recall record at a glance

Official recordF-0956-2021
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmIngredion
Report dateSep 15, 2021
Recall initiation dateAug 6, 2021
Quantity370 kg s
LocationBridgewater, NJ, United States

Official product description

Fermentation Derived Pepsin Product packaging: 5 individual LDPE bags with a net weight of 5kg each and 2.5kg sample bags packaged in 25 kg HDPE Drums

Why the product was recalled

Undeclared egg allergen

Distribution information

Distributed in the following states: CA, MA, FL, WA, UT, TX, ID, CT, IL, and SC.

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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.

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