Wonton Specialist Inc. Dumpling Skin Recall for Undeclared FD&C Red No. 40
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Wonton Specialists is recalling 240 bags of its Dumpling Skin product due to undeclared FD&C Red No. 40.
The full picture behind this FDA recall
This notice was issued by FDA on September 14, 2026 and geographically references New York, New Jersey, Pennsylvania. The FDA classifies this as a Class III recall, with the stated reason "Undeclared FD&C Red No. 40", distributed ny, nj, pa. FDA recall classes run from I (reasonable probability of serious harm) to III (unlikely to cause harm), so the class number is the fastest way to gauge severity here. 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.
It is tempting to skim, check personal relevance, and move on. The better habit is confirming scope, source, and timestamp first, then reading this alongside related notices instead of drawing a conclusion from one record alone.
The original agency source is linked below so you can verify this record directly before acting on it. Its related labels are recall, product-safety, fda, Food.
What Happened
Wonton Specialists has initiated a voluntary recall of Wonton Specialist Inc. Dumpling Skin because the product contains undeclared FD&C Red No. 40.
Which Products Are Affected
The recall involves Wonton Specialist Inc. Dumpling Skin, 16 oz, packaged in foam tray overwrapped with clear plastic. A total of 240 bags are affected. The products were distributed in NY, NJ, and PA. The recall number is H-1324-2026. No codes are associated with the recalled product.
What You Should Do
Consumers should not consume the product if they have sensitivities to FD&C Red No. 40 and should contact Wonton Specialists for additional guidance on returns or refunds.
Why This Matters
Undeclared color additives may affect individuals with sensitivities, though the recall is classified as Class III.
Source
FDA recall H-1324-2026 (https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts)
Original source: FDA Official Notice ↗
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Comparable nationwide notices (length or severity timing) 8
Beyond this FDA recall's own category, Areazine surfaces two nationwide peer sets: length-matched and severity/date-matched notices from elsewhere in the archive, distinct from the same-feed Related list above.
Similar body length
Nearest notices by article body length (920 characters here).
Similar severity timing
Same severity (low) notices issued closest in time to September 14, 2026.
What People Ask
Common questions about this FDA recall.