D'Dioses Vainilla Ice Pop Recall Issued by FDA
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 Vainilla due to possible 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. initiated a voluntary recall of Ice Pop, D'Dioses Vainilla after the product was found to potentially contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Which Products Are Affected
The recall covers Ice Pop, D'Dioses Vainilla, 4 oz (85 g), UPC 710594511829. A total of 144 cases are affected. The product was distributed in NJ, CT, NY and PA. Additional codes listed in the recall: 710594511867,710594511850, 710594511560, 827912008456, 8279120084732, 710594511829, 71059511812, 827912008487, 827912008548, 710594511836, 827912008531, 827912008494, 827912008593, 827912008449, 710594511362,710594511225. Recall number: H-1163-2026. Classification: Class I. Recall initiation date: 20260504.
What You Should Do
Consumers should avoid consuming the recalled product.
Why This Matters
Undeclared allergens and colors in the product pose a serious health risk to individuals with sensitivities or allergies.
Source
FDA recall H-1163-2026 (event ID 99040)
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 (1,026 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.