D'Dioses Rompope 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 Ice Pop, D'Dioses Rompope 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 10, 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. is recalling its Ice Pop, D'Dioses Rompope 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 Rompope, 4 oz (85 g), UPC 710594511812. A total of 111 cases are affected. The products were distributed in NJ, CT, NY and PA.
What You Should Do
Consumers should not eat the recalled product.
Why This Matters
This is a Class I recall, indicating a reasonable probability that the use of or exposure to the product will cause serious adverse health consequences or death.
Source
FDA recall number H-1164-2026
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 (668 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to August 10, 2026.
Frequently Asked Questions
Common questions about this FDA recall.