D'Dioses Arroz con Leche Ice Pops Recall Issued
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D'Dioses Fruit Pops, Inc. is recalling its Ice Pop, D'Dioses Arroz con Leche due to undeclared milk, pecans, pistachios, yellow #5 and red #40.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 9, 2026 and geographically references NJ, CT, NY, PA. 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.
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What Happened D'Dioses Fruit Pops, Inc. is conducting a voluntary recall of Ice Pop, D'Dioses Arroz con Leche because the product may contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Which Products Are Affected The recall involves Ice Pop, D'Dioses Arroz con Leche, 4 oz (85 g), with UPC 710594511843. A total of 216 cases are affected. The product was distributed in New Jersey, Connecticut, New York and Pennsylvania. Additional codes associated with the recall include 710594511867, 710594511850, 710594511560, 827912008456, 8279120084732, 710594511829, 71059511812, 827912008487, 827912008548, 710594511836, 827912008531, 827912008494, 827912008593, 827912008449, 710594511362 and 710594511225. The recall number is H-1160-2026.
What You Should Do Consumers who have purchased the affected product should not consume it. The recalling firm initiated the recall via letter.
Why This Matters Class I recalls indicate a reasonable probability that the use of or exposure to the violative product will cause serious adverse health consequences or death.
Source FDA recall H-1160-2026, report date 20260722.
Original source: FDA Official Notice ↗
Related FDA Recalls
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Similar body length
Nearest notices by article body length (1,149 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to August 9, 2026.
Frequently Asked Questions
Common questions about this FDA recall.