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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.

37,061
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 recallhttps://www.fsis.usda.gov/recalls-alerts/el-eden-import-distributor-corp-recalls-ineligible-pork-cracklings-products-importedPublished September 9, 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 1,461–1,480 of 20,360 recalls

FDA Recall Ongoing Historical recordClass II

Celecoxib Capsules, 200 mg, 500-count bottle, Rx only, Manufactured by: Alembic Pharmaceuticals Limited (Formulation Division), Panelav 389350, Gujarat, India, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, NDC 62332-142-71

by Alembic Pharmaceuticals Limited

Reason
Presence of Foreign Tablets/Capsules; customer complaint found one Tadalafil 5mg tablet inside a sealed 500-count bottle of Celecoxib 200mg capsule
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

LIPMAN FAMILY FARMS

Product
Cucumber Super Selec Repacked by Lipman Produce Hendersonvil…
Reason
Potential Salmonella Contamination
Published
June 18, 2025
Distribution
Product was distributed to AZ, CA, IL, F…

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FDA Recall United States Terminated Historical recordClass I

LIPMAN FAMILY FARMS

Product
PR Cucumber Sliced 2/5# 1/4 Pack Date May 22 Product of USA…
Reason
Potential Salmonella Contamination
Published
June 18, 2025
Distribution
Product was distributed to AZ, CA, IL, F…

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FDA Recall United States Terminated Historical recordClass I

LIPMAN FAMILY FARMS

Product
Cucumber 5lb Repacked by Lipman Produce Hendersonville, NC 2…
Reason
Potential Salmonella Contamination
Published
June 18, 2025
Distribution
Product was distributed to AZ, CA, IL, F…

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FDA Recall United States Terminated Historical recordClass I

LIPMAN FAMILY FARMS

Product
Cucumber Super Selec Repacked by Lipman Produce Hendersonvil…
Reason
Potential Salmonella Contamination
Published
June 18, 2025
Distribution
Product was distributed to AZ, CA, IL, F…

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FDA Recall United States Terminated Historical recordClass I

LIPMAN FAMILY FARMS

Product
Cucumber 24 Ct Repacked by Lipman Produce Hendersonville, NC…
Reason
Potential Salmonella Contamination
Published
June 18, 2025
Distribution
Product was distributed to AZ, CA, IL, F…

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FDA Recall United States Terminated Historical recordClass III

NOW Foods

Product
NOW Nutritional Yeast Powder, Nt. Wt. 10oz. UPC 7 33739 024…
Reason
regular yeast was inadvertently packaged as nutritional yeast
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

R&M TRADING LLC

Product
Instant Milk Tea Brown Sugar Flavor, R&M Refresher brand, B0…
Reason
The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

R&M TRADING LLC

Product
Instant Milk Tea Original Flavor, R&M Refresher brand, B0D71…
Reason
The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

R&M TRADING LLC

Product
Instant Milk Tea Matcha Flavor, R&M Refresher brand, B0D71Y8…
Reason
The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

R&M TRADING LLC

Product
Instant Milk Tea Taro Flavor, R&M Refresher brand, B0D72CMLB…
Reason
The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

R&M TRADING LLC

Product
Instant Milk Tea Honeydew Flavor, R&M Refresher brand, B0D72…
Reason
The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

NRC Nutrition Pty Ltd

Product
Preconception Multi for Women 60 capsules packaged in bliste…
Reason
inconsistent blending of iodine in the product
Published
June 18, 2025
Distribution
Texas, Minnesota, California, Indiana an…

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FDA Recall Ongoing Historical recordClass II

Spectrum Advanced Gel Hand Sanitizer, Ethyl alcohol 70%, 8 FL OZ (236 mL) per bottle, Manufactured for Medline Industries, Inc., Three Lakes Drive, Northfield, IL 60693 USA. NDC: 53329-202-08, UPC 8 88277 34945 5

by Consumer Product Partners, LLC

Reason
Subpotent product: Product has cloudy appearance and tested below assay label claim for 70% Ethyl Alcohol
Published
June 11, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Lacosamide Oral Solution, USP, 10 mg/mL, 200 mL, Rx Only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for: Apotex Corp., Weston FL 33326, NDC 60505-0405-4

by Apotex Corp.

Reason
Defective Container: This recall is being initiated due to a leaking unit stored horizontally.
Published
June 11, 2025
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

Fluoxetine Tablets, USP, 20 mg, 28-count Carton (4x7 Unit-dose), Manufactured by: TORRENT PHARMACEUTIALS LTD., Indrad-382 721 INDIA; Manufactured for: TORRENT PHARMA INC., Basking Ridge, NJ 07920. NDC: 13668-473-91 (Carton); 13668-473-70 (Blister)

by Torrent Pharma Inc.

Reason
CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim acceptable intake limit.
Published
June 11, 2025
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

Fluoxetine Tablets, USP, 20 mg, 30-count bottle, Rx only, Manufactured by: TORRENT PHARMACEUTIALS LTD., Indrad-382 721 INDIA; Manufactured for: TORRENT PHARMA INC., Basking Ridge, NJ 07920. NDC: 13668-473-30

by Torrent Pharma Inc.

Reason
CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim acceptable intake limit.
Published
June 11, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Indomethacin Extended-Release Capsules, USP, 75 mg, 30 capsules (3 x 10 blister cards) per carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217, NDC 68084-411-21 (carton), NDC 68084-411-11 (blister card).

by Amerisource Health Services LLC

Reason
cGMP deviations
Published
June 11, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Country Favor Inc.

Product
Best Taste Brand Salted Shrimp Paste Sauce; ING: Shrimp, sug…
Reason
Product contains undeclared FD&C Red #3
Published
June 11, 2025
Distribution
CT, GA, IL, IN KS, KY, LA, MA, MN, MO, M…

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FDA Recall United States Terminated Historical recordClass I

South Asian Food Inc.

Product
Bengal King Family Pack Vegetable Singara
Reason
Contains undeclared peanut
Published
June 11, 2025
Distribution
Multiple states

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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.