FDA Recall of Negita Cracker- Shrimp Due to Undeclared Ingredient
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Hadson (Toko) Trading Co. Inc. is voluntarily recalling 142 units of Negita Cracker- Shrimp because it contains undeclared FD&C Yellow 6, affecting consumers in several U.S. states.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on May 13, 2026 and geographically references United States. 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 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
Hadson (Toko) Trading Co. Inc. is recalling Negita Cracker- Shrimp 2.8oz due to the presence of undeclared FD&C Yellow 6, which was not listed on the product label.
Which Products Are Affected
The affected product is Negita Cracker- Shrimp 2.8oz, with UPC code 4975934313310 and best by date of 1/6/2027. A total of 142 units are involved in this recall. The product was distributed to the following states: CT, GA, IL, MA, MD, NJ, NY, OH, PA, TX, UT, and VA. The recall number is H-0679-2026.
What You Should Do
Consumers who have the affected product should check for the UPC code 4975934313310 and best by date of 1/6/2027, and follow the firm's initial notification methods, which include email, fax, letter, press release, telephone, or visit, to arrange for return or further instructions.
Why This Matters
This recall addresses potential health risks from undeclared ingredients, which could affect individuals with allergies, highlighting the importance of accurate food labeling for consumer safety.
Source
Attribution: FDA. For more information, visit the FDA website at https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts and search for recall number H-0679-2026.
Original source: FDA Official Notice ↗
Related FDA Recalls
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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 (1,222 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to May 13, 2026.
Frequently Asked Questions
Common questions about this FDA recall.