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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.

37,139
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,799
Class I recallsReasonable probability of serious health consequences
24,349
Class II recallsTemporary or medically reversible health consequences
2,891
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 II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 10,821–10,840 of 21,635 recalls

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

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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

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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

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FDA Recall United States Terminated Historical recordClass I

Northfork Bison Distributions Inc.

Product
Buffalo Burgers ( 100% Pure Canadian Bison Meat ), Net Weig…
Reason
Out of the abundance of caution, NORTHFORK BISON DISTRIBUTIONS INC. IS VOLUNTARILY RECALLING BISON BURGERS & GROUND BECAUSE OF POTENTIAL CONTAMINATION BY E. COLI: 0121 AND 0103.
Published
August 14, 2019
Distribution
GOODS WERE DISTRIBUTED ACROSS THE STATES…

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FDA Recall United States Terminated Historical recordClass II

Brill, Inc., a CSM Bakery Solutions Company - Atlanta Ingredients

Product
48534 MDM 10200921, Natural and Artificial Lemon Flavored Po…
Reason
Frozen, unbaked muffins potentially contaminated with small pieces of plastic.
Published
August 14, 2019
Distribution
Distributed to grocery store distributio…

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FDA Recall United States Terminated Historical recordClass II

Brill, Inc., a CSM Bakery Solutions Company - Atlanta Ingredients

Product
48533 MDM 10200917, Double Dutch Muffin, pre - deposited - u…
Reason
Frozen, unbaked muffins potentially contaminated with small pieces of plastic.
Published
August 14, 2019
Distribution
Distributed to grocery store distributio…

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FDA Recall United States Terminated Historical recordClass I

Wismettac Asian Foods, INC

Product
Shirakiku FISH CAKE SATSUMA AGE SK F; 20/ 150G; Net Wt. 5.2…
Reason
Fish Cake items contain possible contaminating undeclared egg, milk and shellfish.
Published
August 14, 2019
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Wismettac Asian Foods, INC

Product
Shirakiku FISH CAKE AGE BALL SK F; 20/ 150G; Net Wt. 5.29 o…
Reason
Fish Cake items contain possible contaminating undeclared egg, milk and shellfish.
Published
August 14, 2019
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Wismettac Asian Foods, INC

Product
Shirakiku FISH CAKE IKA MAKI SK F; 20/ 150G, Net Wt. 5.29 o…
Reason
Fish Cake items contain possible contaminating undeclared egg, milk and shellfish.
Published
August 14, 2019
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Wismettac Asian Foods, INC

Product
Shirakiku FISH CAKE GOBO MAKI SK F: 20/ 150G, Net Wt. 5.29…
Reason
Fish Cake items contain possible contaminating undeclared egg, milk and shellfish.
Published
August 14, 2019
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Wismettac Asian Foods, INC

Product
Shirakiku FISH CAKE OHBAN AGE SK F; 20/ 150G; Net Wt. 5.29…
Reason
Fish Cake items contain possible contaminating undeclared egg, milk and shellfish.
Published
August 14, 2019
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Wismettac Asian Foods, INC

Product
Shirakuku FISH CAKE MINCH BALL SK F; 20/ 150G; Net Wt. 5.29…
Reason
Fish Cake items contain possible contaminating undeclared egg, milk and shellfish.
Published
August 14, 2019
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Wismettac Asian Foods, INC

Product
Shirakiku FISH CAKE BOUTEN SK F 20/ 150G, Net Wt. 5.29 oz.…
Reason
Fish Cake items contain possible contaminating undeclared egg, milk and shellfish.
Published
August 14, 2019
Distribution
Multiple states

View recall →

FDA Recall United States Terminated Historical recordClass I

Wismettac Asian Foods, INC

Product
Shirakiku FISH CAKE IWASHI TEN SK F 20/150 g; Net WT. 5.29…
Reason
Fish Cake items contain possible contaminating undeclared milk and shellfish.
Published
August 14, 2019
Distribution
Multiple states

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

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FDA Recall United States Terminated Historical recordClass I

Euphoria Fancy Food, Inc.

Product
Tainy Vostoka brand Assorted Dry Fruits-Apple, net wt. 17.63…
Reason
NYS found elevated levels of undeclared Sulfites in Tainy Vostoka Assorted Dry Fruits - Apple.
Published
August 14, 2019
Distribution
NY, NJ, & PA

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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 →

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.