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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

37,066

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,786

Class I recallsReasonable probability of serious health consequences

24,313

Class II recallsTemporary or medically reversible health consequences

2,876

Class III recallsNot likely to cause adverse health consequences

Quick insights

A snapshot of the most notable patterns across all recorded FDA and USDA recalls.

Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap. 53 recalls

Most common hazardLack of Assurance of Sterility 2,072 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026

Most affected stateHawaii 200 recalls mention this state

State: NV ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 13, 2026 ET

Summary (Year to date)

1,527 recalls have been announced year to date.
Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
The highest complete period was Jun 2026 (297).
Sep 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall United States Terminated Historical recordClass II

DAISO CALIFORNIA WAREHOUSE

Product: Wadakan sukiyaki sauce 300ml UPC: 4903636311594
Reason: "Fish" listed in both ingredients list and contains statement; no species identified
Published: May 17, 2023
Distribution: Products were distributed to customer re…

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FDA Recall United States Terminated Historical recordClass III

DAISO CALIFORNIA WAREHOUSE

Product: Ribbon raw thigh candy 65g UPC: 4903316410630
Reason: "Fish" listed in both ingredients list and contains statement; no species identified
Published: May 17, 2023
Distribution: Products were distributed to customer re…

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FDA Recall United States Terminated Historical recordClass III

DAISO CALIFORNIA WAREHOUSE

Product: Daisho Kimchi hotpot soup 750g UPC: 4904621042653
Reason: Label warns for fish but does not specify anchovy or sardine; Canada lists clams in ingredients but not in contains statement.
Published: May 17, 2023
Distribution: Products were distributed to customer re…

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FDA Recall United States Terminated Historical recordClass II

DAISO CALIFORNIA WAREHOUSE

Product: Daisho crab miso soup 750g UPC: 4904621043919
Reason: Contains statement warns for crab but not shrimp (in Flavor)
Published: May 17, 2023
Distribution: Products were distributed to customer re…

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FDA Recall United States Terminated Historical recordClass II

DAISO CALIFORNIA WAREHOUSE

Product: Okabe Funagata small grilled small sardine 43g UPC: 49714550…
Reason: Contains statement warns for sardines instead of anchovy
Published: May 17, 2023
Distribution: Products were distributed to customer re…

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FDA Recall United States Terminated Historical recordClass II

DAISO CALIFORNIA WAREHOUSE

Product: Mangetsu Ebisen 54g UPC: 4901053011370
Reason: Ingredients statement does not list krill; contains statement warns for fish(cuttlefish) and shellfish(shrimp)
Published: May 17, 2023
Distribution: Products were distributed to customer re…

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FDA Recall United States Terminated Historical recordClass III

DAISO CALIFORNIA WAREHOUSE

Product: Nitto Foods Immediately Pickled Dashi 5.5g x 2 Bags UPC: 490…
Reason: Contains statement warns for fish(mackerel, bonito, tuna); ingredients list includes round herring & anchovy
Published: May 17, 2023
Distribution: Products were distributed to customer re…

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FDA Recall United States Terminated Historical recordClass III

DAISO CALIFORNIA WAREHOUSE

Product: Pacifier dried squid cut sea urchin soy sauce flavor 20g U…
Reason: Label lists squid; contains statement lists Fish(squid); other fish not listed in ingredients or contains statement
Published: May 17, 2023
Distribution: Products were distributed to customer re…

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FDA Recall United States Terminated Historical recordClass II

DAISO CALIFORNIA WAREHOUSE

Product: Takuma food dashi salt peanut 80g UPC: 4962679652750
Reason: Products were found to contain flying fish instead of angler fish.
Published: May 17, 2023
Distribution: Products were distributed to customer re…

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FDA Recall United States Terminated Historical recordClass II

DAISO CALIFORNIA WAREHOUSE

Product: Ajikal 44g Kotsubukko 4 series UPC: 4510656600708
Reason: Products were found to contain undeclared coconut
Published: May 17, 2023
Distribution: Products were distributed to customer re…

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FDA Recall United States Terminated Historical recordClass II

DAISO CALIFORNIA WAREHOUSE

Product: Ajikal Age Ichiban 97g UPC: 4510656600906
Reason: Products were found to contain undeclared coconut
Published: May 17, 2023
Distribution: Products were distributed to customer re…

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FDA Recall United States Terminated Historical recordClass I

Euro-Pharma

Product: Multiple Vitamin B Capsules, 60 Capsules, Biologically Activ…
Reason: undeclared allergen (milk)
Published: May 17, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

ZB Importing LLC

Product: Ziyad cinnamon powder, retail 4.5oz plastic jar with shaker…
Reason: Elevated levels of lead
Published: May 17, 2023
Distribution: AL, AR, AZ, CA, CT, DE, FL, IA, IL, IN,…

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FDA Recall Ongoing Historical recordClass I

DYNAMITE SUPER capsule, 58,000 MG, 1-count blister card, Made in America, UPC 6 75799 37602 7.

by Gadget Island, Inc

Reason: Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

NUX Male Enhancement capsule, 1-count blister card, distributed by SX Power CO., Chicago, Il 60612, UPC 6 01577 51236 3.

by Gadget Island, Inc

Reason: Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Pro Power Knight Plus capsule, 2550mg, 1-count blister card, Distributed by Beyond Health and youth Inc, Seattle, WA 98110, UPC 4 94922 90522 0.

by Gadget Island, Inc

Reason: Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Advil Liqui-Gels Solubilized Ibuprofen Capsules, 200 mg Pain Reliever/Fever Reducer (NSAID) a) 20-count Liquid Filled Capsule bottles; b) 40-count Liquid Filled Capsule bottles.

by Family Dollar Stores, Llc.

Reason: CGMP deviation: product outside labeled storage temperature requirements.
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Advil Dual Action with Acetaminophen Acetaminophen 250 mg and Ibuprofen (NSAID) 125 mg Tablets Pain Reliever, 36 Caplets bottles

by Family Dollar Stores, Llc.

Reason: CGMP deviation: product outside labeled storage temperature requirements.
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Advil Ibuprofen Tablets, 200 mg Pain Reliever/Fever Reducer (NSAID) 24-count Caplets

by Family Dollar Stores, Llc.

Reason: CGMP deviation: product outside labeled storage temperature requirements.
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Advil Ibuprofen Tablets, 200 mg Pain Reliever/Fever Reducer (NSAID) packaged in a) 100-count bottles, b) 50-count bottles, and c) 3 (2 count) packets.

by Family Dollar Stores, Llc.

Reason: CGMP deviation: product outside labeled storage temperature requirements.
Published: May 10, 2023
Distribution: Nationwide

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Data last updated: September 13, 2026 ET

Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions. Read the full medical disclaimer.