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
View recall →
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
🇺🇸 United States
Ongoing
Historical recordClass II
FLP LLC
- Product
- Dr. Rico Perez Super Kids Colostrum, 60 count chewable table…
- Reason
- Colostrum is declared but label does not declare milk.
- Published
- May 17, 2023
- Distribution
- Distributed in CA, FL, NJ, and NY.
View recall →
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
View recall →
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
View recall →
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
View recall →
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
View recall →
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
View recall →
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
View recall →
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
View recall →
FDA Recall
Terminated
Historical recordClass II
Simvastatin USP 40 mg, Rx only, Intas Pharm. Limited Ahmedabad 380 054 India Pkg By: PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 a) 30 count-bottle (NDC 43063-0726-30) b) 90 count-bottle (NDC 43063-0726-90)
by PD-Rx Pharmaceuticals, Inc.
- Reason
- CGMP deviations.
- Published
- May 10, 2023
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Simvastatin USP 20 mg, Rx only, Intas Pharm. Limited Ahmedabad 380 054 India Pkg By: PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 a) 30 count-bottles (NDC 43063-008-30), b) 90 count-bottles (NDC: 43063-0008-90)
by PD-Rx Pharmaceuticals, Inc.
- Reason
- CGMP deviations.
- Published
- May 10, 2023
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Glimepiride USP, 4 mg, 90 count-bottles, Rx only, Intas Pharm. Limited Pkg By: PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127, NDC 43063-0587-90
by PD-Rx Pharmaceuticals, Inc.
- Reason
- CGMP deviations.
- Published
- May 10, 2023
- Distribution
- Nationwide
View recall →
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.
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