Yeast Extract Ajirex in 15 kg PE bag in carton box
Summary
The FDA issued a Class II for Yeast Extract Ajirex in 15 kg PE bag in carton box by Mitsubishi International Food Ingredients, Inc.. Reason: Potential Salmonella contamination..
Details
Source
Food Recall
External ID
F-0285-2022
Action Date
2021-12-22
Status
Terminated
Category
food
Product Description
Yeast Extract Ajirex in 15 kg PE bag in carton box
Lot/Code Info: Batch/Lot: AR21B13401 Product Number: 6225796 205 01M Expiration Date: Aug 2, 2022
Quantity Affected: 90 carton boxes.
Reason for Recall
Potential Salmonella contamination.
Distribution
Products were distributed to the following states: GA, IL, PA, & TX. *Firm has been notified by GFS that they did use some of the recalled product in production. GFS is in HAFE3 and has been notified of this situation.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-11-29
Company
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 42 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 (Mitsubishi International Food Ingredients, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Mitsubishi International Food Ingredients, Inc. have FDA actions?
This is the only FDA action we have on record for Mitsubishi International Food Ingredients, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0285-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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