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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

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

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

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

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 4,741–4,760 of 22,291 recalls

FDA Recall United States Terminated Historical recordClass II

Borris Brothers

Product
Smoked Swordfish Dip, Net Wt. 8oz
Reason
Undeclared Yellow #5
Published
May 17, 2023
Distribution
U.S. distribution within state of Florid…

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FDA Recall United States Terminated Historical recordClass II

Borris Brothers

Product
Smoked Wahoo Dip, Net Wt. 8oz
Reason
Undeclared Yellow #5
Published
May 17, 2023
Distribution
U.S. distribution within state of Florid…

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FDA Recall United States Terminated Historical recordClass II

Borris Brothers

Product
Smoked Mahi Dip, Net Wt. 8oz and 48oz
Reason
Undeclared Yellow #5
Published
May 17, 2023
Distribution
U.S. distribution within state of Florid…

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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 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.

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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 Ongoing Historical recordClass II

Seatex Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-Sterile Solution Net Contents: 3.785 L (1 Gallon) Container, UPC 6 12592 01480 0 Seatex, LLC. 445 TX Hwy 36 Rosenberg, TX 77471.

by Seatex LLC

Reason
Superpotent Drug and Failed Impurities/Degradation Products: formula does not adhere to the labeled specifications
Published
May 10, 2023
Distribution
Multiple states

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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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Data last updated:

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.