Fermentation Derived Pepsin Product packaging: 5 individual LDPE bags with a net weight of 5kg each and 2.5kg sample ba
Summary
The FDA issued a Class II for Fermentation Derived Pepsin Product packaging: 5 individual LDPE bags with a ne by Ingredion. Reason: Undeclared egg allergen.
Details
Source
Food Recall
External ID
F-0956-2021
Action Date
2021-09-15
Status
Terminated
Category
food
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
Lot/Code Info: 20352B1 20352B2 21054B1 21054B2 21078B Sample 20223B1 Sample 20223B2 Sample PRTN02000510KFP093B Sample 20101114F14FB15F2F Sample 0201011114F14FB Sample PRTN02000610KFP093B Sample 021B023KFP
Quantity Affected: 370 kg s
Reason for Recall
Undeclared egg allergen
Distribution
Distributed in the following states: CA, MA, FL, WA, UT, TX, ID, CT, IL, and SC.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-08-06
Company
Bridgewater, NJ
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 49 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Ingredion) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Ingredion have FDA actions?
This is the only FDA action we have on record for Ingredion in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0956-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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