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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.

37,115
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,793
Class I recallsReasonable probability of serious health consequences
24,343
Class II recallsTemporary or medically reversible health consequences
2,887
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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 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 II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 8,341–8,360 of 18,020 recalls

FDA Recall Terminated Historical recordClass II

Prostatin Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published
August 14, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Lung Tonic EX Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published
August 14, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Lung Saver Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published
August 14, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Lung Fixer Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published
August 14, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Lube Lax Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published
August 14, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Herpes-V Balm, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published
August 14, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Herpes-S, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published
August 14, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Herpes-G Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published
August 14, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Hair Back, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published
August 14, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Edema Off Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published
August 14, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Dragon Pain Oil, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published
August 14, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Cardia Forte, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published
August 14, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Baby Saver Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published
August 14, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Asthma Balm 60 gram, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published
August 14, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Asma Aid Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

by Herbal Doctor Remedies

Reason
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Published
August 14, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Lovastatin Tablets USP, 40 mg, packaged in a) 100-count bottles (NDC 68001-316-00) and b)1000-count bottles (NDC 68001-316-08), Rx Only, Manufactured by: Lupin Limited, Goa 403 722 INDIA For BluePoint Laboratories.

by American Health Packaging

Reason
CGMP Deviations: Finished product made with lovastatin drug substance that was out of specification for individual impurity results.
Published
August 14, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Mott's LLP

Product
Penafiel Mineral Spring Water 600mL (20.3 FL OZ) and Penafie…
Reason
Elevated levels of inorganic arsenic
Published
August 14, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Drospirenone and Ethinyl Estradiol Tablets, USP, 3 mg/0.02 mg, packaged into a carton containing 3 blister cards each blister card contains 28-film coated, biconvex tablets, Rx Only, Manufactured by: Cyndea Pharma, S.L., Olvega (Soria), 42110 Spain, Distributed by: Jubilant Cadista Pharmaceuticals, Inc., Salisbury, MD, 21801 USA, NDC 59746-763-43

by Jubilant Cadista Pharmaceuticals, Inc.

Reason
Failed dissolution specifications : failed results at the 3-month stability time point.
Published
August 7, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Gablofen (baclofen injection), 50 mcg/mL, Single Use Syringe, Rx only, packaged in a box containing one 1 mL syringe, Distributed by: Primal Critical Care, Inc., 3950 Schelden Circle Bethlehem, PA, 18017, NDC 66794-151-01

by Piramal Critical Care, Inc.

Reason
Failed Impurities/Degradation Specification -This recall is being initiated as a precaution due to the presence of an unknown impurity observed during shelf life of the product.
Published
August 7, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Equate Night-time Sleep Aide (Diphenhydramine HCl), 50 mg, Alcohol Free, Berry Flavor, 12 Fl. Oz. (354 mL), OTC, Distributed by: Walmart Stores, Inc., Bentonville, AR 72716, NDC 49035-330-02, UPC 6 8113117595 1

by LNK International, Inc.

Reason
Microbial contamination of non-sterile product
Published
August 7, 2019
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.