FDA Recall of Doraditas de Azucar Over Allergen Labeling Issue
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Distribuidora de Alimentos Sendero LLC is recalling 500 units of Doraditas de Azucar due to missing wheat and soy allergens on the label, affecting consumers in Texas.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 7, 2026 and geographically references Texas. Its severity classification of "high" 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
Distribuidora de Alimentos Sendero LLC initiated a voluntary recall of Doraditas de Azucar because the product labels do not include wheat and soy as allergens.
Which Products Are Affected
The affected product is Doraditas de Azucar with UPC 5901234123457. The recall involves 500 units distributed in Texas, covering all expiration dates. The recall number is H-0649-2026.
What You Should Do
Consumers should contact the recalling firm, Distribuidora de Alimentos Sendero LLC at their address, 204 Elida St, Mission, TX 78573-3511, for instructions on returns or refunds, as initially notified through methods such as email, fax, letter, press release, telephone, or visit.
Why This Matters
This Class I recall is significant because missing allergen information could lead to serious health risks for individuals with wheat or soy allergies. It highlights the importance of accurate food labeling to prevent potential adverse reactions.
Source
Attribution: FDA. For more information, visit the FDA website and search for recall number H-0649-2026.
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 (1,082 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to April 7, 2026.
Frequently Asked Questions
Common questions about this FDA recall.