Class IITerminatedVoluntary: Firm initiated

Creative Compounds, LLC: food recall H-0900-2026

Creative Compounds, LLC of Scott City, MO recalled Betaine Anhydrous, 2055kg, material packed in foil bags inside 15kg cardboard box Label reads in part as "***BETAINE… Reason: Possible carbon steel foreign material (1-2mm). The FDA listed it as Class II in its Enforcement Report dated Jun 10, 2026; distribution: Florida, Georgia, New Jersey, Oregon, Texas.

Record status as published: Terminated (terminated Jun 22, 2026). openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product: 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***"
Product quantity: 2055 kgs
Reason for recall: Possible carbon steel foreign material (1-2mm)
Codes, lots and dates on the package: Lot Code SWT2025100101 Expiration Date September 2027
Distribution pattern: 5 direct accounts located in FL, NJ, TX, GA and OR
Recalling firm: Creative Compounds, LLC, Scott City, MO
Classification: Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Voluntary or mandated: Voluntary: Firm initiated
How the firm first notified customers: E-Mail

Dates

Event	Date
Recall initiated by the firm	Dec 15, 2025
Classified by the FDA	Jun 2, 2026
Published in the Enforcement Report	Jun 10, 2026
Terminated	Jun 22, 2026

All food recall records

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Sources

U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0900-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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