D'Dioses Grocella Ice Pops 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 46 cases of Ice Pop, D'Dioses Grocella 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 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 conducting 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 involves Ice Pop, D'Dioses Grocella, 1 Bar (81.7 g), with UPC 827912008531. A total of 46 cases are affected. The products were distributed in NJ, CT, NY, and PA. Associated codes include 710594511867, 710594511850, 710594511560, 827912008456, 8279120084732, 710594511829, 71059511812, 827912008487, 827912008548, 710594511836, 827912008531, 827912008494, 827912008593, 827912008449, 710594511362, and 710594511225. This is FDA recall number H-1170-2026, a Class I recall.
What You Should Do
Consumers should not consume the recalled product. Contact the recalling firm or consult FDA resources for further guidance on returns or refunds.
Why This Matters
Class I recalls indicate a reasonable probability that the use of or exposure to the product will cause serious adverse health consequences or death, particularly for individuals with allergies to the undeclared ingredients.
Source
FDA recall H-1170-2026 (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 (1,162 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.