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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.

36,949
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,732
Class I recallsReasonable probability of serious health consequences
24,263
Class II recallsTemporary or medically reversible health consequences
2,873
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 2,071 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)

  • 1,458 recalls have been announced year to date.
  • Aug 2026 was 53% 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 II24,263
Class I9,732
Class III2,873
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,263
Class I9,732
Class III2,873
Not Yet Classified1

Showing 141–160 of 18,300 recalls

FDA Recall Ongoing 2026 recordClass II

Corlanor (ivabradine) tablets, 7.5mg, 60-count bottles, Rx Only, Amgen Inc., Thousand Oaks, CA 92130 Made In Italy. NDC 55513-810-60

by Amgen, Inc.

Reason
Presence of Foreign Substance.
Published
July 1, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Sensipar (cinacalcet) Tablets, 60mg, 30-count bottles, Rx Only, Distributed by: Amge, One Amgen Center Drive, Thousand Oaks ,CA 91320-1799, Made in Japan. NDC 55513-074-30

by Amgen, Inc.

Reason
CGMP Deviations
Published
July 1, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing 2026 recordClass II

Sensipar (cinacalcet) Tablets, 30mg, 30-count bottles, Rx Only, Distributed by: Amge, One Amgen Center Drive, Thousand Oaks ,CA 91320-1799, Made in Japan. NDC 55513-073-30

by Amgen, Inc.

Reason
CGMP Deviations
Published
July 1, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Corlanor (ivabradine) tablets, 5 mg, packaged in a) 14 tablets bottles (NDC 55513-800-99), and b) 60 tablet bottles (NDC 55513-800-60), Rx Only, Amgen Inc., Thousand Oaks, CA 92130 Made In Italy.

by Amgen, Inc.

Reason
Presence of Foreign Substance.
Published
July 1, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Fenofibrate Capsules, USP 200 mg, Rx only, 100 Capsules, Manufactured by: Ajanta Pharma Limited, India, Marketed by: Ajanta Pharma USA Inc. Bridgewater, NJ 08807, NDC 27241-120-04.

by Ajanta Pharma USA Inc

Reason
CGMP Deviations
Published
July 1, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Carton Label: MAJOR, Methylergonovine Maleate Tablets, USP, 0.2 mg, 20 TABLETS (2 x 10), Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, in 46268, NDC 0904-7282-10. Blister Label: Methylergonovine Maleate Tablets, 0.2 mg, USP, One Tablet, Major Pharm/Indianapolis, IN 46268, NDC 0904-7282-10.

by The Harvard Drug Group LLC

Reason
Subpotent Drug
Published
July 1, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

Spring & Mulberry Inc.

Product
Spring & Mulberry Blood Orange Date-Sweetened Chocolate, Net…
Reason
Potential Salmonella contamination
Published
July 1, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

Spring & Mulberry Inc.

Product
Spring & Mulberry Coffee Date-Sweetened Chocolate, Net Wt. 2…
Reason
Potential Salmonella contamination
Published
July 1, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

Spring & Mulberry Inc.

Product
Spring & Mulberry Sea Salt Date-Sweetened Chocolate, Net Wt.…
Reason
Potential Salmonella contamination
Published
July 1, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

Spring & Mulberry Inc.

Product
1) Spring & Mulberry Pure Dark Date-Sweetened Chocolate, Net…
Reason
Potential Salmonella contamination
Published
July 1, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

Spring & Mulberry Inc.

Product
Spring & Mulberry Pecan Date Date-Sweetened Chocolate, Net W…
Reason
Potential Salmonella contamination.
Published
July 1, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

Spring & Mulberry Inc.

Product
Spring & Mulberry Mulberry Fennel Date-Sweetened Chocolate,…
Reason
Potential Salmonella contamination.
Published
July 1, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

Spring & Mulberry Inc.

Product
Spring & Mulberry Mango Chili Date-Sweetened Chocolate, Net…
Reason
Potential Salmonella contamination
Published
July 1, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

Spring & Mulberry Inc.

Product
Spring & Mulberry Lavender Rose Date-Sweetened Chocolate, Ne…
Reason
Potential Salmonella contamination
Published
July 1, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

Spring & Mulberry Inc.

Product
Spring & Mulberry Earl Grey Date-Sweetened Chocolate, Net Wt…
Reason
Potential Salmonella contamination
Published
July 1, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

Spring & Mulberry Inc.

Product
Spring & Mulberry Mixed Berry Date-Sweetened Chocolate, Net…
Reason
Potential Salmonella contamination
Published
July 1, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

Spring & Mulberry Inc.

Product
Spring & Mulberry Mint Leaf Date-Sweetened Chocolate, Net Wt…
Reason
Potential Salmonella contamination
Published
July 1, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass II

Champion Foods, LLC

Product
Motor City Pizza Co. 5 Cheese Bread Single retail pack; 22.4…
Reason
potential salmonella contamination
Published
July 1, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Med Pride, Triple Antibiotic Ointment, Bacitracin Zinc 400 units, Neomycin Sulfate 5 mg, Polymyxin B 5000 units, 1oz (28.3g) tubes, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC 3 52410 30255 8.

by Dabur India Limited

Reason
CGMP Deviations; deficiencies observed during FDA inspection
Published
June 24, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Med Pride, Triple Antibiotic Ointment, Bacitracin Zinc (equivalent to 400 units), Neomycin Sulfate 5 mg, Polymixin B 5000 units, 0.9g packets, 144 packets per box, 130g, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC 1 03 52410 30253 1.

by Dabur India Limited

Reason
CGMP Deviations; deficiencies observed during FDA inspection
Published
June 24, 2026
Distribution
Nationwide

View recall →

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.