Food Recall Check
Class II · Moderate risk Terminated Initiated Aug 6, 2021 (5 years ago)

Fermentation Derived Pepsin Product packaging recall

Recalled by Ingredion · Bridgewater, NJ, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Undeclared egg allergen

Undeclared allergen: Egg

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

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

Quantity: 370 kg s

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

20352B1 20352B2 21054B1 21054B2 21078B Sample 20223B1 Sample 20223B2 Sample PRTN02000510KFP093B Sample 20101114F14FB15F2F Sample 0201011114F14FB Sample PRTN02000610KFP093B Sample 021B023KFP

Where it was sold

California Connecticut Florida Idaho Illinois Massachusetts South Carolina Texas Utah Washington

FDA's distribution note: Distributed in the following states: CA, MA, FL, WA, UT, TX, ID, CT, IL, and SC.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to egg; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Ingredion
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 6, 2021
In FDA report of
Sep 15, 2021
Terminated
Jun 10, 2022
FDA recall number
F-0956-2021 · event 88459
Official record
FDA enforcement report search