D'Dioses Fresa Leche Ice Pop Recall for Undeclared Allergens
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
D'Dioses Fruit Pops, Inc. is recalling 149 cases of Ice Pop, D'Dioses Fresa Leche due to potential 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.
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
D'Dioses Fruit Pops, Inc. initiated a voluntary recall of certain ice pops that may contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Which Products Are Affected
The recall covers Ice Pop, D'Dioses Fresa Leche, 4 oz (85 g), UPC 710594511850. A total of 149 cases are affected. The recall number is H-1159-2026. Additional codes include 710594511867, 710594511850, 710594511560, 827912008456, 8279120084732, 710594511829, 71059511812, 827912008487, 827912008548, 710594511836, 827912008531, 827912008494, 827912008593, 827912008449, 710594511362, 710594511225. The products were distributed in NJ, CT, NY and PA.
What You Should Do
Consumers who have purchased the affected products should not consume them if they have allergies or sensitivities to the undeclared ingredients.
Why This Matters
This is a Class I recall involving undeclared allergens in a food product distributed across multiple states.
Source
FDA recall H-1159-2026, report date 20260722.
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 (1,007 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.