Betaine Anhydrous Recall Issued by Creative Compounds
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Creative Compounds, LLC is recalling 2055 kg of Betaine Anhydrous due to possible carbon steel foreign material.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on July 9, 2026 and geographically references Florida, New Jersey, Texas, Georgia, Oregon. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Food.
What Happened
Creative Compounds, LLC has initiated a voluntary recall of Betaine Anhydrous after discovering possible carbon steel foreign material measuring 1-2mm.
Which Products Are Affected
The recall involves 2055 kg of Betaine Anhydrous 98%, packed in foil bags inside 15 kg cardboard boxes. The label reads in part "***BETAINE ANHYDROUS 98%Distributed by Creative Compounds, LLC Scott City, Missouri USA 63780". Affected product is identified by Lot Code SWT2025100101 with an expiration date of September 2027. The recall number is H-0900-2026. Distribution was limited to 5 direct accounts in FL, NJ, TX, GA and OR.
What You Should Do
Consumers in possession of the recalled product should not use it. The recalling firm initiated the action via e-mail notification.
Why This Matters
This Class II recall addresses a potential foreign material hazard in a food ingredient distributed to multiple states.
Source
FDA Recall H-0900-2026 - Event ID 99015, Report Date 20260610
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,031 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to July 9, 2026.
Frequently Asked Questions
Common questions about this FDA recall.