XZL Jelly Snacks Recall for Undeclared Dyes
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SUNGAL INC is recalling XZL Jelly Snacks due to undeclared FD&C Yellow #5, #6 and Red #40. The recall affects 100 cases distributed in New York and Rhode Island.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on May 24, 2026 and geographically references New York, Rhode Island. Its severity classification of "medium" 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 read it as a data point about the issuing system: how quickly FDA detected the hazard, how precise the geographic or product-identifier scope is, and whether similar notices have clustered in the same category or region in the last 90 days. Cluster patterns frequently precede a broader regulatory action, a single localized FDA recall is isolated; three of them within a quarter often indicate a supply-chain, infrastructure, or seasonal driver that will keep producing notices until something structural changes.
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What Happened
SUNGAL INC has initiated a voluntary recall of XZL Jelly Snacks because the product contains undeclared FD&C Yellow #5 & #6 and Red #40.
Which Products Are Affected
The recall involves XZL Jelly Snacks, 12.68 OZ Bag (12 Bags per Case), UPC CODE 6926475202449. A total of 100 Cases are affected. The product was distributed to NY and RI.
What You Should Do
Consumers should not consume the recalled product.
Why This Matters
Undeclared food dyes may cause allergic reactions in sensitive individuals.
Source
FDA recall H-0689-2026 (https://www.fda.gov)
Original source: FDA Official Notice ↗
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