Azuma Foods Recalls Tako Wasabi for Undeclared Fish
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Azuma Foods International Inc USA is recalling its TAKO WASABI Seasoned Octopus with Wasabi due to undeclared fish, classified as Class I.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 1, 2026 and geographically references United States. 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
Azuma Foods International Inc USA has initiated a voluntary recall of its TAKO WASABI Seasoned Octopus with Wasabi product because it contains undeclared fish.
Which Products Are Affected
The recalled product is azuma foods TAKO WASABI Seasoned Octopus with Wasabi, PERISHABLE/KEEP FROZEN, PRODUCT OF JAPAN, DISTRIBUTED BY: AZUMA FOODS INTERNATIONAL INC., U.S.A. HAYWARD, CA 94545. Retail: 3-50g PACKS NET WT. 5.3 OZ (150g) UPC: 745329900647. Foodservice: 2.2lbs UPC: 745329900746. Retail: 545 cases (12 3-pack units/case); Foodservice: 3616 cases (12 units/case). Distribution in AK, AZ, CA, CO, FL, GA, HI, IL, MD, MA, NC, NJ, NV, NY, OR, TX, WA. Specific lot codes and best by dates are listed in the recall notice.
What You Should Do
Consumers should not consume the product and should return it to the place of purchase or contact the recalling firm for further instructions.
Why This Matters
This is a Class I recall for an undeclared allergen that may cause serious or life-threatening allergic reactions.
Source
FDA recall number H-1075-2026
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 (1,082 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to August 1, 2026.
Frequently Asked Questions
Common questions about this FDA recall.