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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
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 2,601–2,620 of 23,167 recalls

FDA Recall United States Terminated Historical recordClass II

Advance Food International Inc.

Product
Shahzada brand Pulses and Spices; Cinnamon Powder; 7 oz (200…
Reason
Product contains elevated levels of lead (2,030 ppb)
Published
August 28, 2024
Distribution
Multiple states

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FDA Recall Ongoing Historical recordClass II

Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 5mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, Maharashtra, India, Distributed by: Rising Pharmaceuticals Inc, New Jersey, [NDC 64980-514-05].

by FDC Limited

Reason
Defective container; yellow colored spike from cap lodged in the nozzle
Published
August 21, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

North Fish USA, Inc.

Product
Cold Smoked Capelin, 9-ounce packages, plastic trays, 34 pac…
Reason
Clostridium botulinum (uneviscerated fish)
Published
August 21, 2024
Distribution
U.S. distribution to the following: GA a…

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FDA Recall United States Terminated Historical recordClass I

Van Leeuwen Ice Cream LLC

Product
VEGAN OAT; Van Leeuwen PUMPKIN CINNAMON ROLL; NON-DAIRY FROZ…
Reason
Undeclared peanuts (allergen)
Published
August 21, 2024
Distribution
NY

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FDA Recall United States Terminated Historical recordClass II

Pariva LLC

Product
Pariva Marinated Labneh Bites Rosemary Garlic; NET WT 8 OZ (…
Reason
Product may be contaminated with mold.
Published
August 21, 2024
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Pariva LLC

Product
Pariva Marinated Labneh Bites Mild Tandoori; NET WT 8 OZ (22…
Reason
Product may be contaminated with mold.
Published
August 21, 2024
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Pariva LLC

Product
Pariva Marinated Labneh Bites Za'atar; NET WT 8 OZ (225g); I…
Reason
Product may be contaminated with mold.
Published
August 21, 2024
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

RS Hanline and Company Inc

Product
Green Peppers packaged as whole 10lb carton, whole 20lb cart…
Reason
Potential contamination with Listeria monocyotgenes
Published
August 21, 2024
Distribution
Kentucky, New York, Ohio, Pennsylvania,…

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FDA Recall United States Terminated Historical recordClass I

RS Hanline and Company Inc

Product
Poblano packaged as 5lb half sliced with 2 bags per case, 5l…
Reason
Potential contamination with Listeria monocyotgenes
Published
August 21, 2024
Distribution
Kentucky, New York, Ohio, Pennsylvania,…

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FDA Recall United States Terminated Historical recordClass I

RS Hanline and Company Inc

Product
Jalapeno peppers packaged as 5lb diced with 2 bags per case,…
Reason
Potential contamination with Listeria monocyotgenes
Published
August 21, 2024
Distribution
Kentucky, New York, Ohio, Pennsylvania,…

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FDA Recall United States Terminated Historical recordClass I

RS Hanline and Company Inc

Product
Freshire Farms - Green Peppers packaged in plastic bags cont…
Reason
Potential contamination with Listeria monocyotgenes
Published
August 21, 2024
Distribution
Kentucky, New York, Ohio, Pennsylvania,…

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FDA Recall United States Terminated Historical recordClass I

RS Hanline and Company Inc

Product
Freshire Farms - Green Beans packaged in plastic bags at 1lb…
Reason
Potential contamination with Listeria monocyotgenes
Published
August 21, 2024
Distribution
Kentucky, New York, Ohio, Pennsylvania,…

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FDA Recall United States Terminated Historical recordClass I

RS Hanline and Company Inc

Product
Freshire Farms - Jalapenos packaged in plastic bags at 8oz,…
Reason
Potential contamination with Listeria monocyotgenes
Published
August 21, 2024
Distribution
Kentucky, New York, Ohio, Pennsylvania,…

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FDA Recall United States Terminated Historical recordClass III

SUBCO FOODS INC

Product
Fox's u-bet Vanilla Flavored Syrup, 20oz, UPC 070216241016,…
Reason
Customer complaint for bloated bottles. Testing and examination of these lots has revealed they did not meet specifications, including elevated pH and water activity levels. This may be indicative of microbiological activity, and concurrent risk of food-borne illness.
Published
August 21, 2024
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass III

SUBCO FOODS INC

Product
Fox's u-bet Sugar-Free Chocolate Flavored Syrup, 18oz, UPC 0…
Reason
Customer complaint for bloated bottles. Testing and examination of these lots has revealed they did not meet specifications, including elevated pH and water activity levels. This may be indicative of microbiological activity, and concurrent risk of food-borne illness.
Published
August 21, 2024
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

G.S. Gelato and Desserts Inc.

Product
FULL CIRCLE market COCONUTMILK CHOCOLATE ALMOND CRUNCH NON0D…
Reason
Undeclared cashews. The firm was notified by a customer that the top label and the carton labels do not match. The carton label states, "coconut milk" while the top label states, "cashew milk". The product actually contains the cashew milk product.
Published
August 21, 2024
Distribution
The product was shipped to the following…

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FDA Recall Terminated Historical recordClass II

Gabapentin Tablets, USP, 600 mg, 500-count bottles, Rx only, Manufactured by: Granules India Limited Hyderabad-500 081, India, Manufactured for: Granules Pharmaceuticals Inc., Chantilly, VA NDC 70010-227-05

by Granules Pharmaceuticals Inc.

Reason
Presence of Foreign Tablets; 3 fused tablets of Metformin ER 500 mg were found in bottle of Gabapentin Tablets
Published
August 14, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Acetaminophen Extra Strength Tablets, 500 mg each, 100 count bottles, Packaged By: A-S Medication Solutions, Libertyville, IL 60048. NDC: 50090-5313-2

by A-S Medication Solutions LLC

Reason
Labeling: Label Mix-Up: Some bottles of Acetaminophen Extra Strength 500 mg tablets were incorrectly labeled with the drug facts label for Aspirin 81 mg tablets.
Published
August 14, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Empower Pharmacy, Estradiol Cypionate Injection, 10mg/mL, 5mL Sterile Multiple Dose Vial, For IM or SQ use only, RX only, Compounded by: Empower Pharmacy 7601 N Sam Houston Pkwy W Ste 100, Houston, TX 77064

by EMPOWER CLINIC SERVICES LLC

Reason
Lack of Assurance of Sterility
Published
August 14, 2024
Distribution
Nationwide

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FDA Recall Completed Historical recordClass III

Methotrexate Tablets, USP, 2.5mg, 100-count Bottle, RX Only, Distributed By: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC# 69238-1423-1

by Amneal Pharmaceuticals, LLC

Reason
Presence of Foreign Tablets: Potential presence of Fludrocortisone Acetate Tablet USP 0.1 mg within the Methotrexate 2.5 mg 100-count Bottle.
Published
August 14, 2024
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.