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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.

37,059
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/made-fresh-salads-inc-recalls-ready-eat-deli-style-salads-and-cream-cheese-because-possible-healthPublished September 6, 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 641–660 of 20,055 recalls

FDA Recall United States Ongoing 2026 recordClass III

Super World Trading Inc.

Product
MEI HEONG YUEN GARLIC FLAVOR ROASTED PEANUTS; 9.17 oz (260g)…
Reason
Products contain cyclamates (banned sweetener)
Published
April 8, 2026
Distribution
Multiple states

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FDA Recall United States Ongoing 2026 recordClass III

Super World Trading Inc.

Product
MEI HEONG YUEN WALNUT FLAVOR ROASTED PEANUTS; 9.17 oz (260g)…
Reason
Products contain cyclamates (banned sweetener)
Published
April 8, 2026
Distribution
Multiple states

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FDA Recall United States Ongoing 2026 recordClass III

Super World Trading Inc.

Product
MEI HEONG YUEN TANGERINE FLAVOR ROASTED PEANUTS; NET 9.17 oz…
Reason
Products contain cyclamates (banned sweetener)
Published
April 8, 2026
Distribution
Multiple states

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FDA Recall United States Ongoing 2026 recordClass II

JFE FRANCHISING INC

Product
" Dumpling Party Tray (20pcs) Vegetable 13 oz…
Reason
Foreign Object (Glass)
Published
April 8, 2026
Distribution
Multiple states

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FDA Recall United States Ongoing 2026 recordClass II

JFE FRANCHISING INC

Product
" Dumpling Vegetable 4.5 oz…
Reason
Foreign Object (Glass)
Published
April 8, 2026
Distribution
Multiple states

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FDA Recall Ongoing 2026 recordClass II

Meclizine Hydrochloride Tablets, USP 12.5 mg, (a) 50 Tablets [5 x 10] (NDC 60687-775-65) (b) 12.5 mg Individual Dose ( NDC 60687-775-11), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio, 43217.

by Amerisource Health Services LLC

Reason
Failed tablet specifications.
Published
April 1, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 30 mg, Single-dose 8 mL vial in Kit, Rx only, Manufactured in Greece BY: Pharmathen International S.A, Rodopi, 693 00 Greece, Manufactured For: TEVA Pharmaceuticals, Parsippany, NJ 07054, NDC 0480-9262-08.

by Teva Pharmaceuticals USA, Inc

Reason
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
Published
April 1, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 20 mg, Single-dose 8 mL vial in Kit, Rx only, Manufactured in Greece BY: Pharmathen International S.A, Rodopi, 693 00 Greece, Manufactured For: TEVA Pharmaceuticals, Parsippany, NJ 07054, NDC 0480-9259-08.

by Teva Pharmaceuticals USA, Inc

Reason
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
Published
April 1, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 10 mg, Single-dose 8 mL vial in Kit, Rx only, Manufactured in Greece BY: Pharmathen International S.A, Rodopi, 693 00 Greece, Manufactured For: TEVA Pharmaceuticals, Parsippany, NJ 07054, NDC 0480-9257-08.

by Teva Pharmaceuticals USA, Inc

Reason
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
Published
April 1, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Levothyroxine Sodium Tablets USP 150 mcg, 1000 Tablets bottle, Rx Only, Manufactured for: Macleods Pharma USA, Inc., Princeton, NJ, Manufactured by: Macleods Pharmaceuticals Ltd., Sarigam, Valsad, Guajarat, INDIA NDC 33342-401-44

by MACLEODS PHARMA USA, INC

Reason
Subpotent Drug
Published
April 1, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

CUROSURF (poractant alfa), 240 mg, Intratracheal Suspension, 3L Single-dose-Vial, Rx only, Chiesi USA, Inc, Cary, NC 27518, NDC 10122-510-03.

by Chiesi USA, Inc.

Reason
Lack of Assurance of Sterility
Published
April 1, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass III

Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (containing 5 empty capsules and 5 Dibasic Sodium Phosphate Capsules 300 mg, International Isotopes Inc., Idaho Falls, ID 83401. NDC: 69208-003-15; 69208-003-25; 69208-003-35

by Radnostix

Reason
Failed Tablet/Capsule Specifications
Published
April 1, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass II

Bakkavor

Product
Roasted Tomato Parmesan Focaccia Bread sold under the brand…
Reason
Metal fragments in bread. The firm discovered metal fragments in various bread products. They determined the cause to be roasted tomatoes provided by one of their ingredient suppliers.
Published
April 1, 2026
Distribution
Product was shipped to the following sta…

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FDA Recall United States Ongoing 2026 recordClass II

Bakkavor

Product
Basil Pesto & Mozzarella Pizza NET WT. 13.90OZ (394g) UPC 8…
Reason
Metal fragments in bread. The firm discovered metal fragments in various bread products. They determined the cause to be roasted tomatoes provided by one of their ingredient suppliers.
Published
April 1, 2026
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated 2026 recordClass II

Savannah Bee Company Inc.

Product
SAVANNAH BEE COMPANY HONEY BBQ SAUCE MUSTARD NET 16 FL OZ (4…
Reason
Undeclared Allergens: Soy & Wheat. The firm was notified by a customer that the product is labeled as Savannah Bee Company Honey BBQ Sauce "Mustard", but the product inside the bottle is a different flavor of BBQ sauce. After investigation, the firm determined that the product in the bottle is their Honey BBQ Sauce "Sweet". The BBQ sauce "Sweet" contains wheat and soy which is not listed on the BBQ Sauce "Mustard" label.
Published
April 1, 2026
Distribution
Product was shipped to the following sta…

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FDA Recall United States Ongoing 2026 recordClass II

Ajinomoto Foods North America Inc.

Product
Item 6430153 Ajinomoto Vegetable Gyoza Dumplings. Net wt. 24…
Reason
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
Published
April 1, 2026
Distribution
Distributed in AK, AL, AR, AZ, CA, CO, C…

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FDA Recall United States Ongoing 2026 recordClass II

Ajinomoto Foods North America Inc.

Product
Item 6430143 Ajinomoto Vegetable Gyoza Dumplings 12ct. Net w…
Reason
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
Published
April 1, 2026
Distribution
Distributed in AK, AL, AR, AZ, CA, CO, C…

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FDA Recall United States Ongoing 2026 recordClass II

Ajinomoto Foods North America Inc.

Product
Item 6430093 Ajinomoto Green Gyoza Vegetable & Edamame Dumpl…
Reason
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
Published
April 1, 2026
Distribution
Distributed in AK, AL, AR, AZ, CA, CO, C…

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FDA Recall United States Ongoing 2026 recordClass II

Ajinomoto Foods North America Inc.

Product
Item 81153 Kroger Chinese Inspiration Vegetable Fried Rice -…
Reason
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
Published
April 1, 2026
Distribution
Distributed in AK, AL, AR, AZ, CA, CO, C…

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FDA Recall United States Ongoing 2026 recordClass II

Ajinomoto Foods North America Inc.

Product
Item 81146 Ajinomoto Tai Pei Shrimp Fried Rice - Shrimp, veg…
Reason
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
Published
April 1, 2026
Distribution
Distributed in AK, AL, AR, AZ, CA, CO, C…

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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.