Betaine Anhydrous, 2055kg, material packed in foil bags inside 15kg cardboard box Label reads in part as "***BETAINE ANH
Summary
The FDA issued a Class II for Betaine Anhydrous, 2055kg, material packed in foil bags inside 15kg cardboard bo by Creative Compounds, LLC. Reason: Possible carbon steel foreign material (1-2mm).
Details
Source
Food Recall
External ID
H-0900-2026
Action Date
2026-06-10
Status
Terminated
Category
food
Product Description
Betaine Anhydrous, 2055kg, material packed in foil bags inside 15kg cardboard box Label reads in part as "***BETAINE ANHYDROUS 98%***Distributed by Creative Compounds, LLC Scott City, Missouri USA 63780***"
Lot/Code Info: Lot Code SWT2025100101 Expiration Date September 2027
Quantity Affected: 2055 kgs
Reason for Recall
Possible carbon steel foreign material (1-2mm)
Distribution
5 direct accounts located in FL, NJ, TX, GA and OR
Type: Voluntary: Firm initiated
Recall Initiated: 2025-12-15
Company
Scott City, MO
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 166 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 (Creative Compounds, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Creative Compounds, LLC have FDA actions?
This is the only FDA action we have on record for Creative Compounds, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0900-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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