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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: ND ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 12, 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

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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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

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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

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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

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FDA Recall Terminated Historical recordClass II

Simvastatin USP, 10 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 43063-0727-30) b) 90 count-bottle (NDC 43063-0727-90)

by PD-Rx Pharmaceuticals, Inc.

Reason: CGMP deviations.
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Montelukast Sodium USP, 10 mg, 30 count-bottles, Rx only, Intas Pharm, Limited Ahmedabad 380 054 India Pkg By: PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127, NDC 43063-0762-30

by PD-Rx Pharmaceuticals, Inc.

Reason: CGMP deviations.
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Lidocaine Patch 5%, 1 patch (63629-8755-20) packaged in 30-count patches per carton (63629-8755-1), Rx only, each patch contains: 700 mg (50mg per gram adhesive) in an aqueous base, Manufactured by: Actavis Laboratories UT, Inc., Relabeled by: Bryant Ranch Prepack, Inc. Burbank, CA 91504 USA

by Bryant Ranch Prepack, Inc.

Reason: Labeling: Typographical error on the upper left-hand side of the box and individual patch label that has the incorrect dosage form stating, each tablet contains instead of each adhesive patch contains.
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Cargill, Inc Corporate Headquarters

Product: PROSANTE TVGPTN 10BF MNCD 25LB BG/40P, PROSANTE TVGPTN 10BF…
Reason: Products with a gluten free claim may contain gluten levels above 20 ppm.
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Weleda Inc

Product: Hepatodoron¿ tablets, 200 pcs
Reason: Dietary supplement may contain metal
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

SIMPLY GOOD FOODS CO

Product: Atkins Dark Chocolate Royale Protein Rich Shakes, NET WT. 44…
Reason: This recall has been initiated because a contamination event downstream of the thermal process deemed the product not commercially sterile and creates the potential for product spoilage.
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

SIMPLY GOOD FOODS CO

Product: Atkins Milk Chocolate Delight Protein Rich Shakes, NET WT. 4…
Reason: This recall has been initiated because a contamination event downstream of the thermal process deemed the product not commercially sterile and creates the potential for product spoilage.
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Cargill, Inc Corporate Headquarters

Product: PROSANTE TVGPTN 10P MNCD 25LB BG/32P, paper bag
Reason: Products with a gluten free claim may contain gluten levels above 20 ppm.
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Cargill, Inc Corporate Headquarters

Product: PROSANTE TVGPTN 12BF MNCD 50LB BG/36P, paper bag
Reason: Products with a gluten free claim may contain gluten levels above 20 ppm.
Published: May 10, 2023
Distribution: Nationwide

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Data last updated: September 12, 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.